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113495-60-6

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113495-60-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113495-60-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,4,9 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 113495-60:
(8*1)+(7*1)+(6*3)+(5*4)+(4*9)+(3*5)+(2*6)+(1*0)=116
116 % 10 = 6
So 113495-60-6 is a valid CAS Registry Number.

113495-60-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-diphenyl-2,5-dihydroselenophene

1.2 Other means of identification

Product number -
Other names Selenophene,2,5-dihydro-3,4-diphenyl

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:113495-60-6 SDS

113495-60-6Relevant articles and documents

Formation of 2,5-Dihydroselenophenes and 1,3-Dienes from Diketo Selenides by Reduction with Low-valent Titanium Reagents

Nakayama, Juzo,Ikuina, Yoji,Murai, Fumito,Hoshino, Masamatsu

, p. 1072 - 1073 (1987)

Reduction of a series of diketo selenides with a low-valent titanium reagent affords 2,5-dihydroselenophenes and 1,3-dienes in comparable yields.

SYNTHESES WITH DIKETO SELENIDES

Nakayama, Juzo,Shibuya, Masahiro,Ikuina, Yoji,Murai, Fumito,Hoshino, Masamatsu

, p. 149 - 156 (2007/10/02)

We report a) a modified synthesis of diketo selenides, b) preparation of 2,5-diacylselenophenes by condensation of diketoselenides with glyoxal, c) preparation of poly-substituted selenophenes by intramolecular reductive coupling reaction of diketo selenides with low-valent titanium reagent under controlled conditions (0 degC) followed by dehydratation of the resulting 3,4-dihydroxyselenolanes, and d) formation of 2,5-dihydroselenophenes and 1,3-dienes by treatment of diketo selenides with the low-valent titanium reagent in refluxing tetrahydrofuran.

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