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77102-82-0

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77102-82-0 Usage

Uses

3,3'',4,4''-Tetrabromobiphenyl is multi-persistent organic pollutants analyzed in breast milk of first time mothers. An environmental pollutant that affects copper and molybdenum metabolism in rats. Also, it is derived from 1-Bromo-2- nitrobenze (B686175), which is an organic building block used for the synthesis of various pharmaceutical compounds. It is an intermediate for the synthesis of novel Diarylamino-1,3,5-triazine derivatives as FAK inhibitors with anti-angiogenic activity.

Check Digit Verification of cas no

The CAS Registry Mumber 77102-82-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,0 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77102-82:
(7*7)+(6*7)+(5*1)+(4*0)+(3*2)+(2*8)+(1*2)=120
120 % 10 = 0
So 77102-82-0 is a valid CAS Registry Number.

77102-82-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dibromo-4-(3,4-dibromophenyl)benzene

1.2 Other means of identification

Product number -
Other names 3,4,3',4'-Tetrabrom-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:77102-82-0 SDS

77102-82-0Synthetic route

3,3'-dibromo-[1,1'-biphenyl]-4,4'-diamine
34237-98-4

3,3'-dibromo-[1,1'-biphenyl]-4,4'-diamine

3,3',4,4'-tetrabromo-1,1'-biphenyl
77102-82-0

3,3',4,4'-tetrabromo-1,1'-biphenyl

Conditions
ConditionsYield
With sulfuric acid Diazotization.Behandlung der Diazoniumsalz-Loesung mit CuBr in wss. HBr;
1,2-dibromobenzene
583-53-9

1,2-dibromobenzene

3,3',4,4'-tetrabromo-1,1'-biphenyl
77102-82-0

3,3',4,4'-tetrabromo-1,1'-biphenyl

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: (1,5-cyclooctadiene)(methoxy)iridium(l) dimer; 4,4'-di-tert-butyl-2,2'-bipyridine / tetrahydrofuran / 24 h / 80 °C / Inert atmosphere
2: copper diacetate; 1,10-Phenanthroline / N,N-dimethyl-formamide / 12 h / 20 °C
View Scheme
2-(3,4-dibromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
1075719-78-6

2-(3,4-dibromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

3,3',4,4'-tetrabromo-1,1'-biphenyl
77102-82-0

3,3',4,4'-tetrabromo-1,1'-biphenyl

Conditions
ConditionsYield
With 1,10-Phenanthroline; copper diacetate In N,N-dimethyl-formamide at 20℃; for 12h; regioselective reaction;0.218 g

77102-82-0Downstream Products

77102-82-0Relevant articles and documents

Sterically controlled C-H/C-H homocoupling of arenes: Via C-H borylation

Pei, Xiaocong,Zhou, Guan,Li, Xuejing,Xu, Yuchen,Panicker, Resmi C.,Srinivasan, Rajavel

supporting information, p. 5703 - 5707 (2019/06/19)

A mild one-pot protocol for the synthesis of symmetrical biaryls by sequential Ir-catalyzed C-H borylation and Cu-catalyzed homocoupling of arenes is described. The regiochemistry of the biaryl formed is sterically controlled as dictated by the C-H borylation step. The methodology is also successfully extended to heteroarenes. Some of the products obtained by this approach are impossible to obtain via the Ullmann or the Suzuki coupling protocols. Finally, we have shown a one-pot sequence describing C-H borylation/Cu-catalyzed homocoupling/Pd-catalyzed Suzuki coupling to obtain π-extended arene frameworks.

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