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10265-69-7

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10265-69-7 Usage

General Description

Sodium N-phenylglycinate, also known as NPG-Na, is a chemical compound primarily used as an intermediate in the production of pharmaceuticals and agrochemicals. It is a white to off-white crystalline powder that is soluble in water and ethanol. Sodium N-phenylglycinate is also used as a chiral resolving agent in the separation of racemic mixtures and as a catalyst in organic synthesis. It is a relatively stable compound under normal conditions, but should be stored in a cool, dry place away from direct sunlight and heat sources. This chemical has potential uses in various industries and has been found to be an effective and versatile compound in chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 10265-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,6 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10265-69:
(7*1)+(6*0)+(5*2)+(4*6)+(3*5)+(2*6)+(1*9)=77
77 % 10 = 7
So 10265-69-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO2.Na/c10-8(11)6-9-7-4-2-1-3-5-7;/h1-5,9H,6H2,(H,10,11);/q;+1/p-1

10265-69-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,2-anilinoacetate

1.2 Other means of identification

Product number -
Other names Glycine,N-phenyl-,monosodium salt

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:10265-69-7 SDS

10265-69-7Relevant articles and documents

Photoredox-Catalyzed α-Aminomethyl Carboxylation of Styrenes with Sodium Glycinates: Synthesis of γ-Amino Acids and γ-Lactams

Zhou, Cong,Li, Miao,Sun, Jianwei,Cheng, Jiang,Sun, Song

, p. 2895 - 2899 (2021)

A visible-light photoredox-catalyzed reductive α-aminomethyl carboxylation of styrenes with sodium glycinates and CO2 has been developed to synthesize a series of α,α-disubstituted γ-amino acids and γ-lactams with high efficiency and regioselectivity. Notably, CO2 released from the decarboxylation step can be reused for the subsequent carboxylation. Distinct from the previous reactions with the same type of substrates leading to simple decarboxylation and olefin hydroalkylation, this process involves additional CO2 sequestration, thus leading to olefin α-aminomethyl carboxylation. These findings not only provide new access to α,α-disubstituted γ-amino acids and γ-lactams but also serve as a proof of concept for CO2 reutilization in decarboxylation reactions.

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