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101670-65-9

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101670-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101670-65-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,6,7 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 101670-65:
(8*1)+(7*0)+(6*1)+(5*6)+(4*7)+(3*0)+(2*6)+(1*5)=89
89 % 10 = 9
So 101670-65-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H6ClNS/c12-10-5-6-11(13-7-14)9-4-2-1-3-8(9)10/h1-6H

101670-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-4-isothiocyanatonaphthalene

1.2 Other means of identification

Product number -
Other names 4-Chlor-[1]naphthylisothiocyanat

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:101670-65-9 SDS

101670-65-9Relevant articles and documents

2-Arylimino-5,6-dihydro-4H-1,3-thiazines as a new class of cannabinoid receptor agonists. Part 3: Synthesis and activity of isosteric analogs

Kai, Hiroyuki,Morioka, Yasuhide,Koriyama, Yuji,Okamoto, Kazuya,Hasegawa, Yasushi,Hattori, Maki,Koike, Katsumi,Chiba, Hiroki,Shinohara, Shunji,Iwamoto, Yuka,Takahashi, Kohji,Tanimoto, Norihiko

body text, p. 6444 - 6447 (2009/09/30)

Structure-activity relationships and efforts to optimize the pharmacokinetic profile of isosteric analogs of 2-arylimino-5,6-dihydro-4H-1,3-thiazines as cannabinoid receptor agonists are described. Among those examined, compound 25 showed potent affinity for cannabinoid receptor 1 (CB1) and receptor 2 (CB2). This compound displayed oral bioavailability and analgesic activity.

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