Welcome to LookChem.com Sign In|Join Free
  • or
ethyl N-[(3alpha,7alpha,12alpha)-3,7,12-trihydroxy-24-oxocholan-24-yl]aminoacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94006-05-0

Post Buying Request

94006-05-0 Suppliers

Recommended suppliers

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

94006-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94006-05-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,0,0 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94006-05:
(7*9)+(6*4)+(5*0)+(4*0)+(3*6)+(2*0)+(1*5)=110
110 % 10 = 0
So 94006-05-0 is a valid CAS Registry Number.

94006-05-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-[[(4R)-4-[(3R,7R,10S,12S,13R,17R)-3,7,12-trihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoyl]amino]acetate

1.2 Other means of identification

Product number -
Other names EINECS 301-341-0

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:94006-05-0 SDS

94006-05-0Downstream Products

94006-05-0Relevant academic research and scientific papers

METHOD FOR THE SYNTHESIS OF GLYCOCHOLIC ACID

-

Page/Page column 4-5, (2010/11/18)

Process for preparing glycocholic acid comprising the following steps: a) making a mixed anhydride of cholic acid through the suspension of cholic acid in acetone or in aqueous acetone in presence of a base, and subsequent reaction with an alkyl chloroformate; b) aminolysis of the so obtained mixed anhydride of cholic acid with an aqueous solution of a glycine ester, resulting in an ester of glycocholic acid; c) hydrolysis of the ester of glycocholic acid thus obtained through the treatment with aqueous soda or aqueous potassium and precipitation of glycocholic acid through acidification of the corresponding sodium salt.

Chemical modifications of bile acids under high-intensity ultrasound or microwave irradiation

Cravotto, Giancarlo,Boffa, Luisa,Turello, Marta,Parenti, Massimo,Barge, Alessandro

, p. 77 - 83 (2007/10/03)

High-intensity ultrasound (HIU) and microwave (MW) irradiation, having emerged as effective promoters of organic reactions, were exploited for the synthesis of bile acids derivatives. Esterification, amidation, hydrolysis, oxidation, and reduction were investigated. Compared to conventional methods, both techniques proved much more efficient, increasing product yields and dramatically cutting down reaction times. Scaled-up studies are now under way.

Synthesis of linear and cyclic dimeric ester derivatives from bile acids and glycine

Tian, Ze,Cui, Hong,Wang, Yan

, p. 3821 - 3829 (2007/10/03)

Two novel taylor-made linear and cyclic dimers were synthesized from the inexpensive steroid bile acids and amino acid glycine. The structures and stereochemistry of all intermediates and dimers were determined by means of spectroscopic analyses.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 94006-05-0