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16212-85-4

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16212-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16212-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,1 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16212-85:
(7*1)+(6*6)+(5*2)+(4*1)+(3*2)+(2*8)+(1*5)=84
84 % 10 = 4
So 16212-85-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H12S2/c1-3-7-13(8-4-1)15-11-12-16(18-17-15)14-9-5-2-6-10-14/h1-12H

16212-85-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-diphenyldithiine

1.2 Other means of identification

Product number -
Other names 3,6-Diphenyl-1,2-dithiin

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:16212-85-4 SDS

16212-85-4Relevant articles and documents

Novel Synthesis of 3,6-Disubstituted 1,2-Dithiin Molecules Involving a Direct Oxidative Deprotection-Cyclization Sequence from 1,4-Bis(tert-butylthio)-1,3-butadiene Precursors

Koreeda, Masato,Wang, Yamin

, p. 446 - 447 (1997)

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1,2-Dithiines and precursors, XVI: Synthesis, structure, and reactivity of non-anellated 1,2-dithiines

Schroth, Werner,Dunger, Simona,Billig, Frank,Spitzner, Roland,Herzschuh, Rainer,Vogt, Almut,Jende, Thomas,Israel, Gunter,Barche, Jens,Stroehl, Dieter,Sieler, Joachim

, p. 12677 - 12698 (2007/10/03)

Various monocyclic 1,2-dithiines 6a,b,d-t were prepared via (Z,Z)-1,4-difunctionalized butadienes (4-11,19,20). A twisted cyclic structure A is unequivocally proved rather than of the ringopened valence isomer B. The reactivity of these 1,2-dithiines is d

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