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15071-34-8

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15071-34-8 Usage

General Description

(S)-2,3-Dimethylbutanoic acid, also known as isovaleric acid, is a naturally occurring carboxylic acid. It is classified as a branched-chain fatty acid and is commonly found in certain foods and dairy products, as well as in the fermentation process of some types of beer and wine. The compound has a characteristic strong, pungent odor and is frequently used in the production of artificial flavors and fragrances. It is also used in the manufacturing of pharmaceuticals and as a chemical intermediate in the synthesis of various compounds. Additionally, (S)-2,3-Dimethylbutanoic acid has been studied for its potential effects on human health, particularly in relation to its role in body odor and its potential as a biomarker for certain metabolic disorders. Overall, the compound has a diverse range of industrial and biological applications.

Check Digit Verification of cas no

The CAS Registry Mumber 15071-34-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,7 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15071-34:
(7*1)+(6*5)+(5*0)+(4*7)+(3*1)+(2*3)+(1*4)=78
78 % 10 = 8
So 15071-34-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O2/c1-4(2)5(3)6(7)8/h4-5H,1-3H3,(H,7,8)/t5-/m0/s1

15071-34-8SDS

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 (2S)-2,3-dimethylbutanoic acid

1.2 Other means of identification

Product number -
Other names Butanoic acid,2,3-dimethyl

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:15071-34-8 SDS

15071-34-8Relevant articles and documents

Rational Design of Thermodynamic and Kinetic Binding Profiles by Optimizing Surface Water Networks Coating Protein-Bound Ligands

Krimmer, Stefan G.,Cramer, Jonathan,Betz, Michael,Fridh, Veronica,Karlsson, Robert,Heine, Andreas,Klebe, Gerhard

, p. 10530 - 10548 (2016/12/16)

A previously studied congeneric series of thermolysin inhibitors addressing the solvent-accessible S2′ pocket with different hydrophobic substituents showed modulations of the surface water layers coating the protein-bound inhibitors. Increasing stabilization of water molecules resulted in an enthalpically more favorable binding signature, overall enhancing affinity. Based on this observation, we optimized the series by designing tailored P2′ substituents to improve and further stabilize the surface water network. MD simulations were applied to predict the putative water pattern around the bound ligands. Subsequently, the inhibitors were synthesized and characterized by high-resolution crystallography, microcalorimetry, and surface plasmon resonance. One of the designed inhibitors established the most pronounced water network of all inhibitors tested so far, composed of several fused water polygons, and showed 50-fold affinity enhancement with respect to the original methylated parent ligand. Notably, the inhibitor forming the most perfect water network also showed significantly prolonged residence time compared to the other tested inhibitors.

Spirobenzylamine-Phosphine, Preparation Method Therefor And Use Thereof

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Paragraph 0078; 0079, (2014/07/22)

The present invention relates to a spirobenzylamine-phosphine, preparation method therefor and use thereof. The compound has a structure represented by formula (I), wherein n=0 to 3; R1, R2, R3, R4, R5, R6, R7, R8 and R9 having a value as defined in claim 1. Starting from the substituted 7-trifluoromesyloxy-7′-diarylphosphino-1,1′-spiro-dihydroindene, the compound is synthesized in a two-step or three-step reactions. The new spirobenzylamine-phosphine is complexed with an iridium precursor and is subjected to ion exchange, to give an Iridium/spirobenzylamine-phosphine complex comprising various anions. The spiro benzyl amine-phosphine/Iridium complex according to the present invention may be used for catalyzing asymmetry hydrogenation of a variety of alpha-substituted acrylic acids, has high activity and enantio-selectivity, and has a good prospect of industrialization.

CHROMOBACTERIUM FORMULATIONS, COMPOSTIONS, METABOLITES AND THEIR USES

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Page/Page column 26, (2013/05/21)

Stabilized biological pesticides comprising Chromobacterium species, filtrate, supernatant, extract or pesticidally active substance derived therefrom with pesticidal activity having improved shelf life due to maintenance of physical uniformity and longer insecticide activity after use due to higher resistance to degradation when exposed to sunlight are disclosed.

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