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55368-42-8

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55368-42-8 Usage

Chemical Properties

White solid

Uses

4-Bromobenzimidamide, HCl

Check Digit Verification of cas no

The CAS Registry Mumber 55368-42-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,3,6 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 55368-42:
(7*5)+(6*5)+(5*3)+(4*6)+(3*8)+(2*4)+(1*2)=138
138 % 10 = 8
So 55368-42-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H7BrN2.ClH/c8-6-3-1-5(2-4-6)7(9)10;/h1-4H,(H3,9,10);1H

55368-42-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Detail
  • Alfa Aesar

  • (H37831)  4-Bromobenzamidine hydrochloride   

  • 55368-42-8

  • 1g

  • 1221.0CNY

  • Detail
  • Alfa Aesar

  • (H37831)  4-Bromobenzamidine hydrochloride   

  • 55368-42-8

  • 5g

  • 4886.0CNY

  • Detail

55368-42-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Bromobenzamidine hydrochloride

1.2 Other means of identification

Product number -
Other names 4-Bromobenzenecarboximidamide hydrochloride,4-Bromobenzimidamide hydrochloride

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:55368-42-8 SDS

55368-42-8Relevant articles and documents

Silver-catalyzed [3+2+1] annulation of aryl amidines with benzyl isocyanide

Lu, Xiaodong,Xin, Xiaoyi,Wan, Boshun

supporting information, p. 361 - 364 (2018/01/08)

A silver-catalyzed [3+2+1] annulation of amidines with benzyl isocyanide toward 2,4-diaryl-1,3,5-triazines was developed. A variety of symmetrical and unsymmetrical products were obtained in moderate to good yields. This work also features an oxidant-free approach to 2,4-disubstituted triazines.

A 2 - (4 - bromophenyl) -4 - biphenyl -6 - phenyl pyrimidine synthesis method (by machine translation)

-

Paragraph 0010; 0039-0041, (2017/07/22)

The invention belongs to the technical field of organic electroluminescent material, discloses a 2 - (4 - bromophenyl) - 4 - biphenyl - 6 - phenyl pyrimidine synthesis method, the invention organic matter to bromophenylmethyl as raw materials, preparation

Synthesis and structure-activity relationship of 4-amino-2-phenylpyrimidine derivatives as a series of novel GPR119 agonists

Negoro, Kenji,Yonetoku, Yasuhiro,Maruyama, Tatsuya,Yoshida, Shigeru,Takeuchi, Makoto,Ohta, Mitsuaki

experimental part, p. 2369 - 2375 (2012/05/05)

Through preparation and examination of a series of novel 4-amino-2-phenylpyrimidine derivatives as agonists for GPR119, we identified 2-(4-bromophenyl)-6-methyl-N-[2-(1-oxidopyridin-3-yl)ethyl]pyrimidin-4-amine (9t). Compound 9t improved glucose tolerance in mice following oral administration and showed good pharmacokinetic profiles in rats.

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