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383913-41-5

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383913-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 383913-41-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,3,9,1 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 383913-41:
(8*3)+(7*8)+(6*3)+(5*9)+(4*1)+(3*3)+(2*4)+(1*1)=165
165 % 10 = 5
So 383913-41-5 is a valid CAS Registry Number.

383913-41-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-tert-butyl-4-(2-methoxyphenyl)benzene

1.2 Other means of identification

Product number -
Other names 4'-(tert-butyl)-2-methoxy-1,1'-biphenyl

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:383913-41-5 SDS

383913-41-5Relevant articles and documents

The first general palladium catalyst for the Suzuki-Miyaura and carbonyl enolate coupling of aryl arenesulfonates

Nguyen, Hanh Nho,Huang, Xiaohua,Buchwald, Stephen L.

, p. 11818 - 11819 (2007/10/03)

The first general method for the palladium-catalyzed Suzuki-Miyaura and carbonyl enolate coupling of unactivated aryl arenesulfonates was developed utilizing XPhos, 1, and Pd(OAc)2. This is of significant interest because aryl tosylates and aryl benzenesulfonates are more easily handled and considerably less expensive than aryl triflates. This catalyst system effects the coupling of a variety of aryl, heteroaryl, and extremely hindered arylboronic acids with different aryl tosylates, under mild conditions. The same catalyst was employed in the first carbonyl enolate coupling of aryl arensulfonates. Copyright

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