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63619-54-5

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  • Factory wholesale 1,1'-BIPHENYL, 4-BROMO-4'-BUTYL- ;CAS:63619-54-5 CAS NO.63619-54-5

    Cas No: 63619-54-5

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63619-54-5 Usage

Uses

4-Bromo-4'-butyl-1,1'-biphenyl is a useful research chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 63619-54-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,6,1 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 63619-54:
(7*6)+(6*3)+(5*6)+(4*1)+(3*9)+(2*5)+(1*4)=135
135 % 10 = 5
So 63619-54-5 is a valid CAS Registry Number.

63619-54-5SDS

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 4-Bromo-4'-butyl-1,1'-biphenyl

1.2 Other means of identification

Product number -
Other names 1-bromo-4-(4-butylphenyl)benzene

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:63619-54-5 SDS

63619-54-5Relevant articles and documents

Synthesis of unsymmetrically substituted biaryls via sequential lithiation of dibromobiaryls using integrated microflow systems

Nagaki, Aiichiro,Takabayashi, Naofumi,Tomida, Yutaka,Yoshida, Jun-Ichi

supporting information; experimental part, (2010/04/22)

A microflow system consisting of micromixers and microtube reactors provides an effective method for the introduction of two electrophiles onto dibromobiaryls. Selective monolithiation of dibromobiaryls, such as 2,2'-dibromobiphenyl, 4,4'-dibromobiphenyl, 2,7-dibromo-9,9-dioctylfluorene, 2,2'-dibromo-1,1'-binaphthyl, and 2,2'-dibromobibenzyl with 1 equiv of n-butyllithium followed by the reaction with electrophiles was achieved using a microflow system by virtue of fast micromixing and precise temperature control. Sequential introduction of two different electrophiles was achieved using an integrated microflow system composed of four micromixers and four microtube reactors to obtain unsymmetrically substituted biaryl compounds.

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