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3-AMINO-3-(4-NITROPHENYL)PROPIONIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35005-61-9

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35005-61-9 Usage

Purification Methods

The acid crystallises from 50% aqueous EtOH. The hydrochloride has m 218-220o(dec). The N-benzoyl derivative has m 204-205o (from MeOH) and the N-benzoyl-hydrazide has m 226-227o (from MeOH or EtOH). [Posner Justus Liebigs Ann Chem 389 44 1912, Beilstein 14 I 603, 14 IV 1548.]

Check Digit Verification of cas no

The CAS Registry Mumber 35005-61-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,0,0 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 35005-61:
(7*3)+(6*5)+(5*0)+(4*0)+(3*5)+(2*6)+(1*1)=79
79 % 10 = 9
So 35005-61-9 is a valid CAS Registry Number.

35005-61-9 Well-known Company Product Price

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  • Aldrich

  • (573396)  3-Amino-3-(4-nitrophenyl)propionicacid  95%

  • 35005-61-9

  • 573396-1G

  • 957.06CNY

  • Detail

35005-61-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-AMINO-3-(4-NITROPHENYL)PROPIONIC ACID

1.2 Other means of identification

Product number -
Other names 3-<4-Nitro-anilino>-propionsaeure

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:35005-61-9 SDS

35005-61-9Downstream Products

35005-61-9Relevant academic research and scientific papers

Crystal and molecular structure of N-(4-nitrophenyl)-β-alanine - Its vibrational spectra and theoretical calculations

Marchewka,Drozd,Janczak

, p. 758 - 766 (2011)

The N-(4-nitrophenyl)-β-alanine in crystalline form directly by the addition of 4-nitroaniline to the acrylic acid in aqueous solution has been obtained. The title β-alanine derivative crystallizes in the P2 1/c space group of monoclinic system with four molecules per unit cell. The X-ray geometry of β-alanine derivative molecule has been compared with those obtained by molecular orbital calculations corresponding to the gas phase. In the crystal the molecules related by an inversion center interact via symmetrically equivalent O-H?O hydrogen bonds with O?O distance of 2.656(2) forming a dimeric structure. The dimers of β-alanine derivative weakly interact via N-H?O hydrogen bonds between the H atom of β-amine groups and one of O atom of nitro groups. The room temperature powder vibrational (infrared and Raman) measurements are in accordance with the X-ray analysis. In aqueous solution of 4-nitroaniline and acrylic acid, the double CC bond of vinyl group of acrylic acid breaks as result of 4-nitroaniline addition.

Polyclonal antibody-catalysed hydrolysis of a β-lactam

Ostler, Elizabeth L.,Resmini, Marina,Boucher, Guillaume,Romanov, Nickolas,Brocklehurst, Keith,Gallacher, Gerard

, p. 226 - 227 (2002)

We report the first example of antibody-catalysed hydrolysis of a β-lactam where the antibodies were generated by a simple transition-state analogue; in this example the antibodies are polyclonal.

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