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23944-47-0

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23944-47-0 Usage

General Description

2,3-dihydroxy-2-(propan-2-yl)butanoic acid, also known as 2,3-dihydroxy-2-isopropylbutanoic acid, is a chemical compound with the molecular formula C7H14O4. It is a chiral molecule with two stereocenters and can exist in two enantiomeric forms. 2,3-dihydroxy-2-(propan-2-yl)butanoic acid is a derivative of butanoic acid and isopropanol and has two hydroxyl groups attached to the second and third carbons of the carbon chain. It is commonly used as an intermediate in the synthesis of various pharmaceuticals and can also be found in natural products such as plant extracts and microbial metabolites. The compound has potential applications in the pharmaceutical and biotechnology industries due to its structural and functional properties.

Check Digit Verification of cas no

The CAS Registry Mumber 23944-47-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,9,4 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23944-47:
(7*2)+(6*3)+(5*9)+(4*4)+(3*4)+(2*4)+(1*7)=120
120 % 10 = 0
So 23944-47-0 is a valid CAS Registry Number.

23944-47-0SDS

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 2-hydroxy-2-(1-hydroxyethyl)-3-methylbutanoic acid

1.2 Other means of identification

Product number -
Other names -

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:23944-47-0 SDS

23944-47-0Relevant articles and documents

The pheromone system of the male danaine butterfly, Idea leuconoe

Schulz,Nishida

, p. 341 - 349 (2007/10/03)

Male Idea leuconoe butterflies release a complex mixture of volatiles from their pheromone glands (hairpencils) during courtship. The pheromone components geranyl methyl thioether (2), viridifloric β-lactone (3) and 6-hydroxy-4-dodecanolide (10) have been synthesized for the first time. Therefore, the structural assignment of these new natural products could be proved. Related 7-hydroxy-5-alkanolides are also present in the extract. The volatiles are embedded in a lipidic matrix with more than 150 components. This matrix consists of alkanes, alkenes, 2,5-dialkyltetrahydrofurans, secondary alkanols and alkenols as well as alkanones and alkenones. Several regioisomers of the oxidized hydrocarbons occur. The elucidation of double bond positions has been performed by MS using DMDS adducts.

STEREOSELECTIVE REDUCTION OF α-ALKOXY-β-KETO ESTERS. SYNTHESIS OF (+/-)-TRACHELANTHIC ACID AND (+/-)-VIRIDIFLORIC ACID.

Glass, Richard S.,Shanklin, Michael

, p. 545 - 552 (2007/10/02)

Reduction of the isopropylidene derivative of α-hydroxy-α-isopropyl-β-keto-butyric acid 2b with potassium tri(sec.-butyl)-borohydride and zinc borohydride followed by hydrolysis stereoselectivity produces (+/-)-trachelanthic acid, 3, and (+/-)-viridifloric acid, 4, respectively.

The total synthesis of some pyrrolyzidine alkaloids and their absolute configuration.

Kochetkov,Likhosherstov,Kulakov

, p. 2313 - 2323 (2007/10/04)

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