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1795-09-1

1795-09-1

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1795-09-1 Usage

Chemical Properties

Clear colorless to light yellow liquid

Synthesis Reference(s)

Tetrahedron, 31, p. 311, 1975 DOI: 10.1016/0040-4020(75)80039-1Chemical and Pharmaceutical Bulletin, 33, p. 5048, 1985 DOI: 10.1248/cpb.33.5048

Check Digit Verification of cas no

The CAS Registry Mumber 1795-09-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,9 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1795-09:
(6*1)+(5*7)+(4*9)+(3*5)+(2*0)+(1*9)=101
101 % 10 = 1
So 1795-09-1 is a valid CAS Registry Number.

1795-09-1 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (43456)  2-Methyltetrahydrothiophene, 98+%   

  • 1795-09-1

  • 10ml

  • 3141.0CNY

  • Detail

1795-09-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylthiolane

1.2 Other means of identification

Product number -
Other names Thiophene, tetrahydro-2-methyl-

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:1795-09-1 SDS

1795-09-1Relevant articles and documents

HYDROGENATION OF SUBSTITUTED THIOPHENES BY THE Zn-H2SO4 SYSTEM

Latypova, F. M.,Lyakhovetskii, Yu. I.,Lyapina, N. K.,Parnes, Z. N.

, p. 1331 (1985)

-

-

Rigau et al.

, p. 3655,3656, 3657 (1970)

-

E-H (E = R3Si or H) bond activation by B(C6F 5)3 and heteroarenes; Competitive dehydrosilylation, hydrosilylation and hydrogenation

Curless, Liam D.,Clark, Ewan R.,Dunsford, Jay J.,Ingleson, Michael J.

supporting information, p. 5270 - 5272 (2014/05/06)

In the presence of B(C6F5)3 five-membered heteroarenes undergo dehydrosilylation and hydrosilylation with silanes. The former, favoured on addition of a weak base, produces H2 as a by-product making the process catalytic in B(C6F5) 3 but also enabling competitive heteroarene hydrogenation. the Partner Organisations 2014.

Hydrogen storage using heterocyclic compounds: The hydrogenation of 2-methylthiophene

Zhao,Oyama,Naeemi

scheme or table, p. 172 - 184 (2010/11/05)

Alkyl substituted thiophenes are promising candidates for hydrogen carriers, as their dehydrogenation reactions are known to occur under mild conditions. Four types of catalysts, including supported noble metals, bimetallic noble metals, transition metal

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