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2-Amino-1-(4-nitrophenyl)-1,3-propanediol is a chemical compound characterized by its molecular formula C9H12N2O5. It is an amino alcohol with a 1,3-propanediol backbone, featuring an amine and a nitrophenyl substituent. The presence of the nitrophenyl group imparts a distinctive yellow color to the compound, which is useful in various applications.

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  • 119-62-0 Structure
  • Basic information

    1. Product Name: 2-Amino-1-(4-nitrophenyl)-1,3-propanediol
    2. Synonyms: 2-Amino-1-(4-nitrophenyl)-1,3-Propanediol (DL-);2-AMINO-1-(4-NITROPHENYL)-1,3-PROPANEDIOL(DL-)/S-BASE;NSC163951;1-(4'-nitrophenyl)-2-aminopropane-1,3-diol;2-Amino-1-(4-nitrophenyl)-1,3-propanediol;1-(p-Nitrophenyl)-2-amino-1,3-propanediol;2-Amino-3-(4-nitrophenyl)-1,3-propanediol;D-(-)-Three-1-[4-Nitrophenyl]-2-AMino-1,3-Propanediol
    3. CAS NO:119-62-0
    4. Molecular Formula: C9H12N2O4
    5. Molecular Weight: 212.20258
    6. EINECS: 204-338-1
    7. Product Categories: N/A
    8. Mol File: 119-62-0.mol
  • Chemical Properties

    1. Melting Point: 163-165 °C
    2. Boiling Point: 451.881 °C at 760 mmHg
    3. Flash Point: 227.09 °C
    4. Appearance: light yellow crystal power
    5. Density: 1.411 g/cm3
    6. Vapor Pressure: 5.92E-09mmHg at 25°C
    7. Refractive Index: 1.63
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 10.98±0.45(Predicted)
    11. CAS DataBase Reference: 2-Amino-1-(4-nitrophenyl)-1,3-propanediol(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-Amino-1-(4-nitrophenyl)-1,3-propanediol(119-62-0)
    13. EPA Substance Registry System: 2-Amino-1-(4-nitrophenyl)-1,3-propanediol(119-62-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 119-62-0(Hazardous Substances Data)

119-62-0 Usage

Uses

Used in Pharmaceutical Synthesis:
2-Amino-1-(4-nitrophenyl)-1,3-propanediol is utilized as a key intermediate in the synthesis of pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Production:
2-Amino-1-(4-nitrophenyl)-1,3-propanediol is also employed in the production of agrochemicals, contributing to the development of new pesticides and other agricultural products that can enhance crop protection and yield.
Used in Organic Compound Synthesis:
2-Amino-1-(4-nitrophenyl)-1,3-propanediol serves as a versatile building block in the synthesis of various organic compounds, expanding the scope of chemical research and development.
Used in Dye and Pigment Manufacturing:
The characteristic yellow color of 2-Amino-1-(4-nitrophenyl)-1,3-propanediol makes it a valuable colorant in the manufacturing of dyes and pigments for different industries, including textiles, plastics, and printing inks.
Used in Antimicrobial and Antifungal Applications:
2-Amino-1-(4-nitrophenyl)-1,3-propanediol has been studied for its potential biological activities, such as antimicrobial and antifungal properties. It can be used as an active ingredient in the development of new antimicrobial and antifungal agents to combat resistant strains and improve public health.

Check Digit Verification of cas no

The CAS Registry Mumber 119-62-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 119-62:
(5*1)+(4*1)+(3*9)+(2*6)+(1*2)=50
50 % 10 = 0
So 119-62-0 is a valid CAS Registry Number.
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

119-62-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(p-Nitrophenyl)-2-amino-1,3-propanediol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:119-62-0 SDS

119-62-0Relevant articles and documents

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)

Chloramphenicol (CHL) is a ribosome-targeting antibiotic that binds to the peptidyl transferase center (PTC) of the bacterial ribosome and inhibits peptide bond formation. As an approach for modifying and potentially improving the properties of this inhib

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

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.

, (2021)

In the current work, in continuation of our recent research, we synthesized and studied new chimeric compounds, including the ribosome-targeting antibiotic chloramphenicol (CHL) and the membrane-penetrating cation triphenylphosphonium (TPP), which are lin

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)

Florfenicol is the 3′-fluoro derivative of thiamphenicol and has been widely used in veterinary medicine for its high antibacterial activity and safety. However, the development of simplified and environmentally friendly catalytic methods for the stereoselective production of florfenicol is a key challenge. Herein, we established a highly stereoselective enzymatic one-pot reaction for the synthesis of an aminodiol intermediate of florfenicol bearing two stereocenters from industrial raw material 4-(methylsulfonyl) benzaldehyde by coupling transketolase (TK) and ω-transaminase (TA). The enantioselectivity of TK from E. coli was converted from (S) (93% ee) to (R) (95% ee), and we also inverted the enantiopreference (E(S) = 9 to E(R) = 12) and ketone/aldehyde substrate selectivity of TA ATA117 via structure-guided enzyme engineering. Docking calculations and molecular dynamics simulations of the wild-type and mutant enzymes unveiled the molecular basis for enzymatic stereocontrol. Using the engineered TK and TA, (1R,2R)-p-methylsulfonyl phenylserinol was biosynthesized with good yield (76%) and high stereoselectivity (96% de and >99% ee). Our work established an enzymatic synthetic route to (1R,2R)-p-methylsulfonyl phenylserinol, facilitating the development of a chemoenzymatic method for producing florfenicol.

Synthesis of chloramphenicol via a new intermediate 4-para-nitrophenyl- 5-formamido-1,3-dioxane

Hazra, Braja G.,Pore, Vandana S.,Maybhate, Shailaja P.

, p. 1857 - 1864 (1997)

4-Phenyl-5-amino-1,3-dioxane 4, obtained from β-bromo styrene 2 was protected as formamido derivative 5. Nitration of 5 followed by regioselective acylative cleavage of the nitro product 12 gave N-formyl-N- acetyl hemiacetal diacetate 16, which on sequential base and acid hydrolysis followed by dichloroacetylation gave chloramphenicol 1.

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

-

, (2019/01/04)

Provided are engineered polypeptides that are useful for the asymmetric synthesis of β-hydroxy-α-amino acids under industrial-relevant conditions. The engineered polypeptides disclosed are developed through directed evolution based on the ability of catalytic synthesis of (2S, 3R) -2-amino-3-hydroxy-3- (4-nitrophenyl) propanoic acid. Also provided are polynucleotides encoding the engineered polypeptides, host cells capable of expressing engineered polypeptides, and methods of producing β-hydroxy-α-amino acids using engineered polypeptides. Compared to other processes of preparation, the use of the engineered polypeptides for the preparation of β-hydroxy-α-amino acids results in high purity of the desired stereoisomers, mild reaction conditions, low pollution and low energy consumption. It has good industrial application prospects.

Stereocontrolled synthesis of syn-β-hydroxy-α-amino acids by direct aldolization of pseudoephenamine glycinamide

Seiple, Ian B.,Mercer, Jaron A. M.,Sussman, Robin J.,Zhang, Ziyang,Myers, Andrew G.

supporting information, p. 4642 - 4647 (2014/05/20)

β-Hydroxy-α-amino acids figure prominently as chiral building blocks in chemical synthesis and serve as precursors to numerous important medicines. Reported herein is a method for the synthesis of β-hydroxy- α-amino acid derivatives by aldolization of pseudoephenamine glycinamide, which can be prepared from pseudoephenamine in a one-flask protocol. Enolization of (R,R)- or (S,S)-pseudoephenamine glycinamide with lithium hexamethyldisilazide in the presence of LiCl followed by addition of an aldehyde or ketone substrate affords aldol addition products that are stereochemically homologous with L- or D-threonine, respectively. These products, which are typically solids, can be obtained in stereoisomerically pure form in yields of 55-98 %, and are readily transformed into β-hydroxy-α-amino acids by mild hydrolysis or into 2-amino-1,3-diols by reduction with sodium borohydride. This new chemistry greatly facilitates the construction of novel antibiotics of several different classes. On aldol: Enolization of (R,R)- or (S,S)-pseudoephenamine glycinamide with lithium hexamethyldisilazide (LiHMDS) in the presence of LiCl followed by addition of either an aldehyde or ketone substrate affords aldol addition products which are stereochemically homologous with L- or D-threonine, respectively. These products can be obtained in stereoisomerically pure form in yields of 55-98 %, and are readily transformed into β-hydroxy-α-amino acids by mild hydrolysis or into 2-amino-1,3-diols by reduction.

Stereoselective synthesis of (-)-chloramphenicol, (+)-thiamphenicol and (+)-sphinganine via chiral tricyclic iminolactone

Li, Qiong,Zhang, Hongbo,Li, Chenguang,Xu, Pengfei

, p. 149 - 153 (2013/08/24)

The stereoselective syntheses of (-)-chloramphenicol, (+)-thiamphenicol and (+)-sphinganine are described. The two continuous chiral centers within three target molecules were constructed through aldol reaction of chiral tricyclic iminolactone and aldehyde. Concise and efficient syntheses of (-)-chloramphenicol, (+)-thiamphenicol and (+)-sphinganine have been accomplished in practical four or three steps. The synthetic route featured in an aldol reaction between iminolactone 1a and 1b with aldehyde, which introduced the two continuous chiral centers within three target molecules. Copyright

Experimental and DEE study of the conversion of ephedrine derivatives into oxazolidinones. Double SN2 mechanism against SN1 mechanism

El Moncef, Abdelkarim,El Hadrami, El Mestafa,González, Miguel A.,Zaballos, Elena,Zaragozá, Ramón J.

body text, p. 5173 - 5184 (2010/08/22)

Sulfonation of the N-Boc derivatives of 1,2-aminoalcohols, such as ephedrine, pseudoephedrine, norephedrine, norpseudoephedrine, thiomicamine, and chloramphenicol yields a mixture of the corresponding oxazolidinones with inversion (erythro derivatives) and!or retention of configuration (threo derivatives)at C5. We suggest a competition between two mechanisms: an intramolecular SN2 process initiated by attack of the carbonyl oxygen of the Boc group to the benzylic carbon and the other one through a double SN2 process. In the erythro derivatives the first mechanism is predominant, while in the threo derivatives both mechanisms have similar energy. This hypothesis is supported by theoretical calculations and additional experimental assays.

Method of Preparing Clopidogrel and Intermediates Used Therein

-

Page/Page column 5, (2008/12/08)

Optically pure clopidogrel can be prepared in a high yield by optically resolving a racemic form of the compound of formula (II) using an optically active amine to form the optically active form of the compound of formula (III) or its acid-addition salt; and methylating the compound of formula (III) or its acid-addition salt.

Straightforward access to protected syn α-amino-β-hydroxy acid derivatives

Patel, Jignesh,Clave, Guillaume,Renard, Pierre-Yves,Franck, Xavier

supporting information; experimental part, p. 4224 - 4227 (2009/03/12)

(Chemical Equation Presented) Titanium stability: syn α-Amino-β- hydroxy acid derivatives were prepared in excellent diastereoselectivities by an aldol reaction with chiral N-(azidoacetyl)thiazolidin-2-thione derivatives (see scheme; NMP = N-methylpyrrolidinone). Titanium enolates of these derivatives are stable and provide a new and efficient method to access chiral amino acids.

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