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99092-03-2

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99092-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99092-03-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,0,9 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 99092-03:
(7*9)+(6*9)+(5*0)+(4*9)+(3*2)+(2*0)+(1*3)=162
162 % 10 = 2
So 99092-03-2 is a valid CAS Registry Number.

99092-03-2SDS

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 methyl 1-(aminomethyl)cyclopentanecarboxylate

1.2 Other means of identification

Product number -
Other names 1-Aminomethyl-cyclopentanecarboxylic acid methyl ester

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:99092-03-2 SDS

99092-03-2Relevant articles and documents

Substituted cycloalkyls as inhibitors of a beta protein production

-

, (2008/06/13)

This invention relates to novel lactams having the Formula (I): to their pharmaceutical compositions and to their methods of use. These novel compounds inhibit the processing of amyloid precursor protein and, more specifically, inhibit the production of Aβ-peptide, thereby acting to prevent the formation of neurological deposits of amyloid protein. More particularly, the present invention relates to the treatment of neurological disorders related to β-amyloid production such as Alzheimer's disease and Down's Syndrome.

N,N-Bis(trimethylsilyl)methoxymethylamine as a Convenient Synthetic Equivalent for +CH2NH2: Primary Aminomethylation of Esters

Okano, Kohji,Morimoto, Toshiaki,Sekiya, Minoru

, p. 883 - 884 (2007/10/02)

The introduction of a primary aminomethyl unit at the α position of esters can be achieved in high yield by the silyl trifluoromethanesulphonate-catalysed reaction of ketene silyl acetals (2) with N,N-bis(trimethylsilyl)methoxymethylamine (1).

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