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41635-77-2

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41635-77-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41635-77-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,6,3 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 41635-77:
(7*4)+(6*1)+(5*6)+(4*3)+(3*5)+(2*7)+(1*7)=112
112 % 10 = 2
So 41635-77-2 is a valid CAS Registry Number.

41635-77-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name hexa-1,3-dien-1-ylbenzene

1.2 Other means of identification

Product number -
Other names Benzene, 1,3-hexadienyl-

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:41635-77-2 SDS

41635-77-2Relevant articles and documents

Migratory Hydrogenation of Terminal Alkynes by Base/Cobalt Relay Catalysis

Liu, Bingxue,Liu, Qiang,Liu, Xufang

supporting information, p. 6750 - 6755 (2020/03/13)

Migratory functionalization of alkenes has emerged as a powerful strategy to achieve functionalization at a distal position to the original reactive site on a hydrocarbon chain. However, an analogous protocol for alkyne substrates is yet to be developed. Herein, a base and cobalt relay catalytic process for the selective synthesis of (Z)-2-alkenes and conjugated E alkenes by migratory hydrogenation of terminal alkynes is disclosed. Mechanistic studies support a relay catalytic process involving a sequential base-catalyzed isomerization of terminal alkynes and cobalt-catalyzed hydrogenation of either 2-alkynes or conjugated diene intermediates. Notably, this practical non-noble metal catalytic system enables efficient control of the chemo-, regio-, and stereoselectivity of this transformation.

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