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84276-16-4

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84276-16-4 Usage

General Description

D-2-Aminodecanoic acid, also known as 2-Aminocapric acid, is a compound with the chemical formula C10H21NO2. It is an organic compound belonging to the class of amines and carboxylic acids. This chemical is primarily used in the production of pharmaceuticals, specifically as a building block for the synthesis of various drugs. It can also be utilized in the production of surfactants and chelating agents, as well as in biochemical research. D-2-Aminodecanoic acid plays a significant role in the development of certain pharmaceuticals and has varied applications in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 84276-16-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,2,7 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 84276-16:
(7*8)+(6*4)+(5*2)+(4*7)+(3*6)+(2*1)+(1*6)=144
144 % 10 = 4
So 84276-16-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H21NO2/c1-2-3-4-5-6-7-8-9(11)10(12)13/h9H,2-8,11H2,1H3,(H,12,13)

84276-16-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-aminodecanoic acid

1.2 Other means of identification

Product number -
Other names D-2-Aminodecanoic acid

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:84276-16-4 SDS

84276-16-4Relevant articles and documents

A new type of chiral-pyridoxamines for catalytic asymmetric transamination of α-keto acids

Chen, Jianfeng,Zhao, Junyu,Gong, Xing,Xu, Dongfang,Zhao, Baoguo

supporting information, p. 4612 - 4615 (2016/09/23)

A new type of chiral pyridoxamines bearing an adjacent chiral stereocenter has been developed via multi-step synthesis. The pyridoxamines displayed catalytic activity in asymmetric transamination of α-keto acids to give a variety of optically active amino acids in 27–78% yields with 34–62% ee's under very mild conditions. This work provides a synthetic strategy to construct new chiral pyridoxamines using bromopyridine 7 as a key synthon and also represents an early example of the applications of chiral pyridoxamines in asymmetric catalysis.

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