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Mevaldic acid, also known as 3,5-dimethyl-1,4-pentanedioic acid, is an organic compound that serves as a key intermediate in the synthesis of mevalonate, a crucial precursor in the production of cholesterol, steroid hormones, and other essential biomolecules. It is a white crystalline solid with a molecular formula of C7H12O4 and a molecular weight of 160.17 g/mol. Mevaldic acid is synthesized through various chemical reactions, including the condensation of acetone and acetic acid, and plays a significant role in the pharmaceutical industry for the production of statins, a class of drugs used to lower cholesterol levels. Its chemical properties and reactivity make it an important compound in organic synthesis and drug development.

541-07-1

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541-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 541-07-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,4 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 541-07:
(5*5)+(4*4)+(3*1)+(2*0)+(1*7)=51
51 % 10 = 1
So 541-07-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O4/c1-6(10,2-3-7)4-5(8)9/h3,10H,2,4H2,1H3,(H,8,9)

541-07-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name mevaldic acid

1.2 Other means of identification

Product number -
Other names <2-14C>-Mevaldinsaeure

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:541-07-1 SDS

541-07-1Downstream Products

541-07-1Relevant academic research and scientific papers

A CONVERGENT ENANTIOCONTROLLED ROUTE TO MEVALONOLACTONE AND VITAMIN E FROM (S)-O-BENZYLGLYCIDOL

Takano, Seiichi,Shimazaki, Youichi,Iwabuchi, Yoshiharu,Ogasawara, Kunio

, p. 3619 - 3622 (2007/10/02)

A convergent enantiocontrolled route to (+) and (-)-mevalonolactones and vitamin E has been developed using (S)-O-benzylglycidol as the sole chiral block.

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