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3,5-dibromo-2-phenylthiophene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38071-55-5

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38071-55-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38071-55-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,0,7 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 38071-55:
(7*3)+(6*8)+(5*0)+(4*7)+(3*1)+(2*5)+(1*5)=115
115 % 10 = 5
So 38071-55-5 is a valid CAS Registry Number.

38071-55-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dibromo-2-phenylthiophene

1.2 Other means of identification

Product number -
Other names 3,5-dibromo-2-phenyl-thiophene

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:38071-55-5 SDS

38071-55-5Relevant academic research and scientific papers

One-Pot Halogen Dance/Negishi Coupling of Dibromothiophenes for Regiocontrolled Synthesis of Multiply Arylated Thiophenes

Okano, Kentaro,Sunahara, Kazuhiro,Yamane, Yoshiki,Hayashi, Yuki,Mori, Atsunori

supporting information, p. 16450 - 16454 (2016/11/11)

One-pot halogen dance/Negishi cross-coupling of readily available 2,5-dibromothiophenes is described. A lithium diisopropylamide (LDA)-mediated halogen dance reaction resulted in the formation of thermodynamically stable α-lithiodibromothiophenes, which w

Brominated thiophenes as precursors in the preparation of brominated and arylated anthraquinones

Thiemann, Thies,Tanaka, Yasuko,Iniesta, Jesus

experimental part, p. 1013 - 1031 (2009/10/10)

Brominated anthraquinones can be synthesized directly from bromothiophenes when these are reacted with 1,4-naphthoquinones in the presence of meta-chloroperoxybenzoic acid. The bromoanthraquinones are versatile building blocks in the preparation of arylated anthraquinones and of extended π-systems with interspersed anthraquinone units.

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