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108912-09-0

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108912-09-0 Usage

General Description

3-[4-(BROMOMETHYL)PHENYL]THIOPHENE, also known as BMPT, is a chemical compound with a molecular structure consisting of a thiophene ring with a bromomethylphenyl group attached to the third carbon atom. It is commonly used in the synthesis of organic compounds and pharmaceuticals, particularly as a building block in the production of various materials and products. BMPT is known for its reactivity and versatility, making it a valuable intermediate in the chemical industry for the production of various functionalized thiophene derivatives. This chemical compound has potential applications in the fields of medicine, materials science, and organic synthesis due to its unique structural and chemical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 108912-09-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,9,1 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 108912-09:
(8*1)+(7*0)+(6*8)+(5*9)+(4*1)+(3*2)+(2*0)+(1*9)=120
120 % 10 = 0
So 108912-09-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H9BrS/c12-7-9-1-3-10(4-2-9)11-5-6-13-8-11/h1-6,8H,7H2

108912-09-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[4-(BROMOMETHYL)PHENYL]THIOPHENE

1.2 Other means of identification

Product number -
Other names -

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:108912-09-0 SDS

108912-09-0Relevant articles and documents

Preparation and characterization of poly[2,3-dimethyl-1-(4-thien-3-ylbenzyl)-1H-imidazol-3-ium] bis((trifluoromethyl)sulfonyl)imide

Naudin, Eric,Ho, Hoang Anh,Bonin, Marc-Andre,Breau, Livain,Belanger, Daniel

, p. 4983 - 4987 (2002)

A new 3-fluorophenylthiophene derivative bearing a cationic imidazolium group in the para position of the phenyl ring was synthesized by a multistep procedure which involves, in a key step, the reaction of 3-[4-(bromomethyl)phenyl]thiophene with 1,2-dimet

Endothelin receptor antagonists

-

, (2008/06/13)

The present invention provides novel compounds represented by the general formula I: STR1 wherein R 1 is a straight or branched lower alkyl, a cycloalkyl-lower alkyl, an aryl-lower alkyl, a cycloalkyl, an aryl an aryl-cycloalkyl, lower alkoxy, an aryloxy, or a heteroaryl;R 2 is hydrogen, a straight or branched lower alkyl, a cycloalkyl, or a cycloalkyl-lower alkyl;R 3 and R 3 '' are each the same or different and each is hydrogen atom, a straight or branched lower alkyl, a cycloalkyl, an aryl-lower alkyl, an aryl, or a heteroaryl; orR 3 and R 3 '' together form a ring structure;R 3 "" is hydrogen, lower alkyl or an aryl; orR 2 and R 3 "" together form a lower alkylene group --(CH 2) n -- wherein n is an integer of 1, 2 or 3; orR 2 and R 3 "" together form a group represented by the formula: --(CH 2) p --Ar-- or --Ar--(CH 2) p --, respectively, wherein p is zero or an integer of 1 or 2, and Ar is an arylene or heteroarylene;C( X) is C( O), C( S), C( NH), C( N-lower alkyl); C NH--OH, or CH 2 ;Y is a direct bond, --NH--, a lower alkyl-N, an oxygen atom, or methylene; orC( X) is CHOH and Y is a direct bond or methylene;R 4 is --(CH 2) s --Ar'' wherein s is zero or an integer of 1, 2 or 3; and Ar'' is an aryl, or a heteroaryl; andR 5 is carboxy, substituted or unsubstituted carboxamide, PO(OH) 2, tetrazole, CH 2 OH, CN, or hydrogen;and salts thereof.

Benzo-fused lactams promote release of growth hormone

-

, (2008/06/13)

There are disclosed certain novel compounds identified as benzo-fused lactams STR1 which promote the release of growth hormone in humans and animals. This property can be utilized to promote the growth of food animals to render the production of edible meat products more efficient, and in humans, to increase the stature of those afflicted with a lack of a normal secretion of natural growth hormone. The compounds are prepared by substitution of an amino-lactam with a substituted amide function. Growth promoting compositions containing such benzo-fused lactams as the active ingredient thereof are also disclosed.

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