What is the CAS number for (R*,R*)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol?

The CAS number of (R*,R*)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol is 3689-55-2.

What is the CAS number for (R*,R*)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol?

The CAS number of (R*,R*)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol is 3689-55-2.

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(R,R)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol

Q: What is the (R*,R*)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol?

(R*,R*)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol is , while it's Molecular Formula is C 9 H 12 N 2 O 4 . Used in Pharmaceutical Synthesis: (R,R)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol is used as a chiral building block for the production of antibiotics and other drugs. Its unique structure enables the creation of complex molecules with specific properties, contributing to the development of novel therapeutic agents. Used in Chromatography: In the field of analytical chemistry, (R,R)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol serves as a chiral resolving agent in chromatography. This application aids in the separation and identification of enantiomers, which is crucial for understanding the different biological activities and potential side effects of chiral drugs. Used in Asymmetric Catalysis: (R,R)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol is also utilized as a building block in the synthesis of chiral ligands for asymmetric catalysis. These ligands are essential in enhancing the selectivity and efficiency of chemical reactions, leading to the production of enantiomerically pure compounds with desired properties. Used in High-Performance Liquid Chromatography (HPLC): In the development of chiral stationary phases for HPLC, (R,R)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol is employed to create advanced separation techniques. These techniques are vital for the analysis and purification of chiral compounds, which are prevalent in the pharmaceutical, agrochemical, and fragrance industries. Used in the Chemical Industry: (R,R)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol is used as a key intermediate in the synthesis of various organic compounds. Its versatility and reactivity make it a valuable asset in the development of new materials and chemicals with specific applications in different industries.

Q: What is (R*,R*)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol (3689-55-2) used for?

(R,R)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol, with the molecular formula C9H13NO5, is a chiral compound that plays a significant role in the pharmaceutical and chemical industries. Its unique structure allows it to be a versatile building block for various applications.InChI:InChI=1/C9H12N2O4/c10-8(5-12)9(13)6-1-3-7(4-2-6)11(14)15/h1-4,8-9,12-13H,5,10H2

CAS：3689-55-2
purity：99%

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Quality Manufacturer Supply High Purity 99% (R,R)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol 3689-55-2 with Reasonable Price

Molecular Formula: C₉H₁₂N₂O₄
Molecular Weight: 212.205
Melting Point: 143-145 °C
Boiling Point: 451.9°Cat760mmHg
PKA: 10.98±0.45(Predicted)
Flash Point: 227.1°C
PSA： 112.30000
Density: 1.41g/cm³
LogP: 1.17130

(R,R)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol(Cas 3689-55-2) Usage

General Description

(R*,R*)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol is a chemical compound with the molecular formula C9H13NO5. It is a chiral compound that is often used in the synthesis of pharmaceuticals and organic compounds. (R*,R*)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol is commonly used in the production of antibiotics and other drugs due to its role as a chiral building block. It is also used as a chiral resolving agent in chromatography and as a building block in the synthesis of chiral ligands for asymmetric catalysis. Additionally, it has been used in the development of chiral stationary phases for high-performance liquid chromatography.

InChI:InChI=1/C9H12N2O4/c10-8(5-12)9(13)6-1-3-7(4-2-6)11(14)15/h1-4,8-9,12-13H,5,10H2

3689-55-2 Relevant articles

Binding and action of triphenylphosphonium analog of chloramphenicol upon the bacterial ribosome

Chen, Chih-Wei,Pavlova, Julia A.,Lukianov, Dmitrii A.,Tereshchenkov, Andrey G.,Makarov, Gennady I.,Khairullina, Zimfira Z.,Tashlitsky, Vadim N.,Paleskava, Alena,Konevega, Andrey L.,Bogdanov, Alexey A.,Osterman, Ilya A.,Sumbatyan, Natalia V.,Polikanov, Yury S.

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Chloramphenicol (CHL) is a ribosome-targ...

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Abad, Etna,Antonenko, Yuri N.,Bogdanov, Alexey A.,Kajiwara, Susumu,Khairullina, Zimfira Z.,Konevega, Andrey L.,Lukianov, Dmitrii A.,Lyakhovich, Alex,Makarov, Gennady I.,Murayama, Somay Y.,Nazarov, Pavel A.,Osterman, Ilya A.,Paleskava, Alena,Pavlova, Julia A.,Skvortsov, Dmitry A.,Sumbatyan, Natalia V.,Tereshchenkov, Andrey G.,Volynkina, Inna A.

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In the current work, in continuation of ...

One-Pot Asymmetric Synthesis of an Aminodiol Intermediate of Florfenicol Using Engineered Transketolase and Transaminase

Deng, Zixin,Huang, Tingting,Lin, Shuangjun,Liu, Qi,Shi, Ting,Tang, Mancheng,Tao, Wentao,Xie, Xinyue,Zhang, Yuanzhen,Zhao, Yilei

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Florfenicol is the 3′-fluoro derivative ...

ENGINEERED POLYPEPTIDES AND THEIR APPLICATIONS IN SYNTHESIS OF BETA-HYDROXY-ALPHA-AMINO ACIDS

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, (2019/01/04)

Provided are engineered polypeptides tha...

3689-55-2 Process route

: 56-75-7,85666-84-8
chloramphenicol

: 119-62-0,716-61-0,2792-51-0,2792-52-1,2964-48-9,3689-55-2,63526-31-8,71115-69-0,140694-64-0
(1R,2R)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol

Conditions

Conditions	Yield
With sodium hydroxide;
With hydrogenchloride;
With water; sodium hydroxide;
With hydrogenchloride; Heating;
With hydrogenchloride; In water; at 100 ℃; for 2h;

: 1194757-37-3
(2S ,3S )-2-amino-3-hydroxy-3-(4-nitro-phenyl)-propionic acid ethyl ester

: 119-62-0,716-61-0,2792-51-0,2792-52-1,2964-48-9,3689-55-2,63526-31-8,71115-69-0,140694-64-0
(1R,2R)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol

Conditions

Conditions	Yield
ueber mehrere Stufen;

3689-55-2 Upstream products

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(2S ,3S )-2-amino-3-methoxy-3-(4-nitro-phenyl)-propan-1-ol
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(1R ,2S )-2-acetylamino-1-(4-nitro-phenyl)-propane-1,3-diol
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(1S,2S)-2-acetamido-1-phenylpropane-1,3-diyl diacetate

3689-55-2 Downstream products

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(R,R)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol

Quality Manufacturer Supply High Purity 99% (R,R)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol 3689-55-2 with Reasonable Price

(R,R)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol(Cas 3689-55-2) Usage

3689-55-2 Relevant articles

Binding and action of triphenylphosphonium analog of chloramphenicol upon the bacterial ribosome

Chen, Chih-Wei,Pavlova, Julia A.,Lukianov, Dmitrii A.,Tereshchenkov, Andrey G.,Makarov, Gennady I.,Khairullina, Zimfira Z.,Tashlitsky, Vadim N.,Paleskava, Alena,Konevega, Andrey L.,Bogdanov, Alexey A.,Osterman, Ilya A.,Sumbatyan, Natalia V.,Polikanov, Yury S.

, (2021/04/23)

Triphenilphosphonium analogs of chloramphenicol as dual-acting antimicrobial and antiproliferating agents

, (2021/05/10)

One-Pot Asymmetric Synthesis of an Aminodiol Intermediate of Florfenicol Using Engineered Transketolase and Transaminase

Deng, Zixin,Huang, Tingting,Lin, Shuangjun,Liu, Qi,Shi, Ting,Tang, Mancheng,Tao, Wentao,Xie, Xinyue,Zhang, Yuanzhen,Zhao, Yilei

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ENGINEERED POLYPEPTIDES AND THEIR APPLICATIONS IN SYNTHESIS OF BETA-HYDROXY-ALPHA-AMINO ACIDS

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, (2019/01/04)

3689-55-2 Process route

3689-55-2 Upstream products

3689-55-2 Downstream products

Related products

Others

Product classification

Contact us

(R*,R*)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol

Quality Manufacturer Supply High Purity 99% (R*,R*)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol 3689-55-2 with Reasonable Price

(R*,R*)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol(Cas 3689-55-2) Usage

3689-55-2 Relevant articles

Binding and action of triphenylphosphonium analog of chloramphenicol upon the bacterial ribosome

Chen, Chih-Wei,Pavlova, Julia A.,Lukianov, Dmitrii A.,Tereshchenkov, Andrey G.,Makarov, Gennady I.,Khairullina, Zimfira Z.,Tashlitsky, Vadim N.,Paleskava, Alena,Konevega, Andrey L.,Bogdanov, Alexey A.,Osterman, Ilya A.,Sumbatyan, Natalia V.,Polikanov, Yury S.

, (2021/04/23)

Triphenilphosphonium analogs of chloramphenicol as dual-acting antimicrobial and antiproliferating agents

, (2021/05/10)

One-Pot Asymmetric Synthesis of an Aminodiol Intermediate of Florfenicol Using Engineered Transketolase and Transaminase

Deng, Zixin,Huang, Tingting,Lin, Shuangjun,Liu, Qi,Shi, Ting,Tang, Mancheng,Tao, Wentao,Xie, Xinyue,Zhang, Yuanzhen,Zhao, Yilei

, p. 7477 - 7488 (2021/06/30)

ENGINEERED POLYPEPTIDES AND THEIR APPLICATIONS IN SYNTHESIS OF BETA-HYDROXY-ALPHA-AMINO ACIDS

-

, (2019/01/04)

3689-55-2 Process route

3689-55-2 Upstream products

3689-55-2 Downstream products

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(R,R)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol

Quality Manufacturer Supply High Purity 99% (R,R)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol 3689-55-2 with Reasonable Price

(R,R)-(±)-2-amino-1-(p-nitrophenyl)propane-1,3-diol(Cas 3689-55-2) Usage