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35822-49-2

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35822-49-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35822-49-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,2 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35822-49:
(7*3)+(6*5)+(5*8)+(4*2)+(3*2)+(2*4)+(1*9)=122
122 % 10 = 2
So 35822-49-2 is a valid CAS Registry Number.

35822-49-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (1Z,3Z)-1,4-bis(methylsulfanyl)buta-1,3-diene

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:35822-49-2 SDS

35822-49-2Downstream Products

35822-49-2Relevant articles and documents

Synthesis and properties of novel medium-sized heterocyclic compounds containing two sulfur atoms in the ring and synthetic approaches to conjugated cyclic disulfonium ylides

Shimizu, Hiroshi,Watanabe, Hiroyoshi,Mizuno, Masahiro,Kataoka, Tadashi,Hori, Mikio

, p. 139 - 150 (2007/10/03)

Tribenzo[bf,h][1,4]dithiecin (8) was prepared by coupling 2,2'- bis(bromomethyl)biphenyl (10) with 1,2-benzenedithiol (11) in the presence of Nail in acetonitrile. Another novel dithiecin derivative, 1,8-dihydro-2,7benzodithiecin (9) was synthesized by coupling of 1,4-dimercapto-2,3-Oisopropylidene-Lg-threitol (13a) with α,α'-dibromo-o-xylene (12), followed by hydrolysis and subsequent dehydration via the mesylate derivative (16). The benzodithiecin (9) was also prepared by treatment of dithiol (18) with butadiyne along with α,α'-bis(1-buten-3-ynylthio)-o-xylene (19) as a byproduct. Compound (19) was subjected to an intramolecular coupling reaction using CuCl-pyridine-O2 in benzene to yield the 12-membered ring compound (23). We also describe our effort to prepare the corresponding cyclic diylide compounds from the above new dithiecins (8) and (9), and known dithiecin (7).

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