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41085-77-2

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41085-77-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41085-77-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,0,8 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 41085-77:
(7*4)+(6*1)+(5*0)+(4*8)+(3*5)+(2*7)+(1*7)=102
102 % 10 = 2
So 41085-77-2 is a valid CAS Registry Number.

41085-77-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-nitro-5-(5-nitrothiophen-2-yl)thiophene

1.2 Other means of identification

Product number -
Other names 5,5'-Dinitrobithienyl

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:41085-77-2 SDS

41085-77-2Downstream Products

41085-77-2Relevant articles and documents

MECHANISM OF THE ELECTROCHEMICAL REDUCTION OF 2-HALO-5-NITROTHIOPHENES IN DIMETHYLFORMAMIDE

Sosonkin, I. M.,Strogov, G. N.,Ponomareva, T. K.,Domarev, A. N.,Glushkova, A. A.,Freidlin, G. N.

, p. 137 - 140 (1981)

The reduction of 2-bromo-5-nitrothiophene and 2-iodo-5-nitrothiophene in dimethylformamide (DMF) was studied by means of classical and commutated polarography, EPR spectroscopy, a rotating platinum disk electrode with a ring, and preparative electrolysis.It was established that, depending on the nature of the halogen, their anion radicals may undergo further reduction to 2-nitrothiophene anion radicals or decomposition with splitting out of a halide anion and conversion to nitrothienyl radicals, which were identified on the ring electrode.The latter are capable of undergoing dimerization to 2,2'-dinitro-5,5'-dithienyl.The spectra of the anion radicals of 2-nitrothiophene and 2,2'-dinitro-5,5'dithienyl were recorded by means of EPR.A mechanism for the reduction of halonitrothiophenes is proposed.

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