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104901-43-1

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104901-43-1 Usage

Chemical Properties

Orange-red solid

Uses

It is a pharmaceutical intermediate.

Synthesis Reference(s)

The Journal of Organic Chemistry, 53, p. 5545, 1988 DOI: 10.1021/jo00258a030

Check Digit Verification of cas no

The CAS Registry Mumber 104901-43-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,9,0 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104901-43:
(8*1)+(7*0)+(6*4)+(5*9)+(4*0)+(3*1)+(2*4)+(1*3)=91
91 % 10 = 1
So 104901-43-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H9BrO2/c1-6-3-4-7(5-8(6)10)9(11)12-2/h3-5H,1-2H3

104901-43-1 Well-known Company Product Price

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  • (Code)Product description
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  • Detail
  • Alfa Aesar

  • (B24372)  Methyl 3-bromo-4-methylbenzoate, 99%   

  • 104901-43-1

  • 5g

  • 428.0CNY

  • Detail
  • Alfa Aesar

  • (B24372)  Methyl 3-bromo-4-methylbenzoate, 99%   

  • 104901-43-1

  • 25g

  • 1574.0CNY

  • Detail
  • Alfa Aesar

  • (B24372)  Methyl 3-bromo-4-methylbenzoate, 99%   

  • 104901-43-1

  • 100g

  • 3001.0CNY

  • Detail

104901-43-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3-bromo-4-methylbenzoate

1.2 Other means of identification

Product number -
Other names Methyl 3-Bromo-4-Methylbenzoate

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:104901-43-1 SDS

104901-43-1Relevant articles and documents

Aromatic Bromination Using BrF with No Friedel-Crafts Catalyst

Rozen, Shlomo,Brand, Michael,Lidor, Rami

, p. 5545 - 5547 (1988)

-

Cross-coupling strategy for the synthesis of diazocines

Eleya, Nadi,Li, Shuo,Staubitz, Anne

supporting information, p. 1624 - 1627 (2020/03/13)

Ethylene bridged azobenzenes are novel, promising molecular switches that are thermodynamically more stable in the (Z) than in the (E) configuration, contrary to the linear azobenzene. However, their previous synthetic routes were often not general, and yields were poorly reproducible, and sometimes very low. Here we present a new synthetic strategy that is both versatile and reliable. Starting from widely available 2-bromobenzyl bromides, the designated molecules can be obtained in three simple steps.

GLUCOSE-SENSITIVE ALBUMIN-BINDING DERIVATIVES

-

Page/Page column 151; 152, (2019/05/30)

This invention relates to glucose-sensitive albumin-binding diboron conjugates. More particularly the invention provides novel diboron compounds, and in particular diboronate or diboroxole compounds, useful as intermediate compounds for the synthesis of diboron conjugates. The diboron compounds are characterized by formula (I), which is: R1-X-R2, and wherein "X" is a mono- to multiatomic linker and where R1 and R2, which may be identical or different, each represents a group of Formula (lla) or (IIb) Also described are diboron conjugates represented by the general Formula (I'), which is: R1'-X'-R2', in which either the moeities R1' or R2' or X' carry a drug that is covalently attached to the diboron compound.

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