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77269-66-0

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77269-66-0 Usage

Uses

It is used as pharmaceutical intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 77269-66-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,6 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 77269-66:
(7*7)+(6*7)+(5*2)+(4*6)+(3*9)+(2*6)+(1*6)=170
170 % 10 = 0
So 77269-66-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O4/c1-7(11(12)13)4-8-2-3-9-10(5-8)15-6-14-9/h2-3,5,7H,4,6H2,1H3,(H,12,13)

77269-66-0 Well-known Company Product Price

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  • Alfa Aesar

  • (H27924)  2-Methyl-3-[(3,4-methylenedioxy)phenyl]propionic acid   

  • 77269-66-0

  • 1g

  • 613.0CNY

  • Detail
  • Alfa Aesar

  • (H27924)  2-Methyl-3-[(3,4-methylenedioxy)phenyl]propionic acid   

  • 77269-66-0

  • 5g

  • 1883.0CNY

  • Detail

77269-66-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-3-[(3,4-methylenedioxy)phenyl]propionic acid

1.2 Other means of identification

Product number -
Other names 3-(1,3-benzodioxol-5-yl)-2-methylpropanoic acid

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:77269-66-0 SDS

77269-66-0Relevant articles and documents

Synthesis of 2-Arylethylamines by the Curtius Rearrangement

Schulze, Matthias

experimental part, p. 1461 - 1476 (2010/07/08)

2-Arylethylamine derivatives were synthesized using the Curtius reaction and with three different methods of preparing the acyl azide functional group. Carbamates derived from isocyanate were convenient protecting groups for alkylation of amines. Starting from benzaldehyde, amphetamine was prepared in three steps through an oxazolidin-2-one intermediate in 62% overall yield. Copyright Taylor & Francis Group, LLC.

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