Welcome to LookChem.com Sign In|Join Free

CAS

  • or

56434-66-3

Post Buying Request

56434-66-3 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

56434-66-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56434-66-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,4,3 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56434-66:
(7*5)+(6*6)+(5*4)+(4*3)+(3*4)+(2*6)+(1*6)=133
133 % 10 = 3
So 56434-66-3 is a valid CAS Registry Number.

56434-66-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Methyl-c-2-phenyl-r-1-cyclopropancarbonsaeure-methylester

1.2 Other means of identification

Product number -
Other names (1R,2R)-1-Methyl-2-phenyl-cyclopropanecarboxylic acid methyl ester

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:56434-66-3 SDS

56434-66-3Downstream Products

56434-66-3Relevant articles and documents

Palladium-catalyzed methylation and arylation of sp2 and sp 3 C-H bonds in simple carboxylic acids

Giri, Ramesh,Maugel, Nathan,Li, Jiao-Jie,Wang, Dong-Hui,Breazzano, Steven P.,Saunders, Lindsey B.,Yu, Jin-Quan

, p. 3510 - 3511 (2007/10/03)

The use of preformed sodium carboxylates as substrates led to the first observation of facile Pd-insertions into sp3 β-C-H bonds in simple aliphatic acids. Consequently, Pd-catalyzed methylation and arylation of o-C-H bonds in benzoic acids and β-C-H bonds in aliphatic acids using either a phenylboronate, methylboronic acid, or ArI have been achieved via a C-H activation/C-C coupling sequence. Copyright

Deprotonation and Diastereoselective Alkylation of Methyl Cyclopropanecarboxylates

Reichelt, Ingrid,Reissig, Hans-Ulrich

, p. 3895 - 3914 (2007/10/02)

Using model compounds it is demonstrated when deprotonation of methyl cyclopropanecarboxylates leads to ester condensation products and when alkylation of the ester enolate can be performed.Under certain structural conditions (steric and electronic effect

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 56434-66-3