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1008139-18-1

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1008139-18-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1008139-18-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,8,1,3 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1008139-18:
(9*1)+(8*0)+(7*0)+(6*8)+(5*1)+(4*3)+(3*9)+(2*1)+(1*8)=111
111 % 10 = 1
So 1008139-18-1 is a valid CAS Registry Number.

1008139-18-1SDS

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 tert-butyl N-(2-methyl-5-nitropyridin-3-yl)carbamate

1.2 Other means of identification

Product number -
Other names tert-butyl 2-methyl-5-nitropyridin-3-ylcarbamate

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:1008139-18-1 SDS

1008139-18-1Downstream Products

1008139-18-1Relevant articles and documents

PYRIDYLTRIAZOLES

-

Page/Page column 53, (2011/10/13)

The present invention encompasses compounds of general formula (1) wherein the groups R0 to R3 and L are defined as in claim 1, which are suitable for the treatment of diseases characterised by excessive or abnormal cell proliferation, pharmaceutical preparations which contain such compounds and their use as medicaments.

Microwave-assisted synthesis of novel (5-nitropyridin-2-yl)alkyl and (5-nitropyridin-3-yl)alkyl carbamates

Henry, Christophe,Haupt, Andreas,Turner, Sean C.

supporting information; experimental part, p. 1932 - 1938 (2009/08/07)

A straightforward approach to novel (5-nitropyridin-2-yl)alkyl and (5-nitropyridin-3-yl)alkyl carbamate building blocks is presented in this study. Their construction is achieved by condensation of N-carbamate a- and β-amino carbonyl derivatives with l-methyl-3,5-dinitro-2-pyridone 1 under microwave irradiation. Judiciously chosen modifications in the nature of the parent carbonyl starting material has influenced the regiochemical outcome of the reaction and allowed an efficient access to novel nitrogen-containing scaffolds. Compounds sharing morphological similarities have been gathered in three libraries differing from each other in a single structural parameter.

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