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Carbamic acid, (1,2,3,4-tetrahydro-2-oxo-3-quinolinyl)-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

194611-73-9

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194611-73-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 194611-73-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,6,1 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 194611-73:
(8*1)+(7*9)+(6*4)+(5*6)+(4*1)+(3*1)+(2*7)+(1*3)=149
149 % 10 = 9
So 194611-73-9 is a valid CAS Registry Number.

194611-73-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-Oxo-1,2,3,4-tetrahydroquinolin-3-yl)-carbamic acid tert-butyl ester

1.2 Other means of identification

Product number -
Other names 3-t-butyloxycarbonylamino-3,4-dihydrocarbostyril

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:194611-73-9 SDS

194611-73-9Relevant academic research and scientific papers

Conformationally restricted arginine analogues as inhibitors of human nitric oxide synthase

Shearer, Barry G.,Lee, Shuliang,Franzmann, Karl W.,White, Helen A.R.,Sanders, Daniella C.J.,Kiff, Rachel J.,Garvey, Edward P.,Furfine, Eric S.

, p. 1763 - 1768 (1997)

Conformationally restricted analogues of the endogenous NOS substrate L- arginine and the arginine based NOS inhibitors N(G)-methyl-L-arginine (L- NMA) and Nδ-iminoethyl-L-ornithine (L-NIO) were synthesized for evaluation as inhibitors of human NOS. Incorporation of a phenyl ring into the C4-C5 backbone chain provided 2-aminophenylalanine analogues which retained potent NOS inhibition. Structurally related analogues of 3-aminophenylalanine were significantly weaker inhibitors.

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