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Pyridine, 2-methyl-6-nitroso- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

688035-62-3

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688035-62-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 688035-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,8,0,3 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 688035-62:
(8*6)+(7*8)+(6*8)+(5*0)+(4*3)+(3*5)+(2*6)+(1*2)=193
193 % 10 = 3
So 688035-62-3 is a valid CAS Registry Number.

688035-62-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-6-nitrosopyridine

1.2 Other means of identification

Product number -
Other names -

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:688035-62-3 SDS

688035-62-3Upstream product

688035-62-3Relevant academic research and scientific papers

Syntheses and biological evaluation of ring-C modified colchicine analogs

Yang, Baiyuan,Zhu, Zhiqing C.,Goodson, Holly V.,Miller, Marvin J.

scheme or table, p. 3831 - 3833 (2010/08/20)

Ring-C modified alkaloids were synthesized from colchicine using iminonitroso Diels-Alder reactions in a highly regio- and stereoselective fashion. Several analogs exhibited cytotoxic activity similar to that of colchicine itself against PC-3 and MCF-7 cancer cell lines, by serving as prodrugs of colchicine through retro Diels-Alder reactions under the assayed conditions. In vitro microtubule polymerization assays indicated that these modifications affected their interaction with tubulin.

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