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103971-60-4

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103971-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103971-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,9,7 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 103971-60:
(8*1)+(7*0)+(6*3)+(5*9)+(4*7)+(3*1)+(2*6)+(1*0)=114
114 % 10 = 4
So 103971-60-4 is a valid CAS Registry Number.

103971-60-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-bis(phenylselenyl) octane

1.2 Other means of identification

Product number -
Other names 2,2-bis(phenylseleno)octane

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:103971-60-4 SDS

103971-60-4Relevant articles and documents

Highly regioselective palladium-catalyzed double hydroselenation of terminal alkynes with benzeneselenol in the presence of acetic acid

Ikeda, Takuma,Tamai, Taichi,Daitou, Masayuki,Minamida, Yoshiaki,Mitamura, Takenori,Kusano, Hiroki,Nomoto, Akihiro,Ogawa, Akiya

, p. 1383 - 1385 (2013/11/19)

Palladium diacetate (Pd(OAc)2), in the presence of acetic acid, is found to exhibit excellent catalytic activity for the double hydroselenation of terminal alkynes with benzeneselenol to yield the corresponding diselenoketals regioselectively.

The first example of transitionmetal-catalyzed hydroselenation of acetylenes

Kuniyasu, Hitoshi,Ogawa, Akiya,Sato, Ken-Ichiro,Ryu, Iihyong,Sonoda, Noboru

, p. 5525 - 5528 (2007/10/02)

A variety of transition metal complexes catalyzed the regioselective hydroselenation of acetylenes. In particular, the palladium acetate-catalyzed reaction afforded the Markovnikov adducts with high selectivity.

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