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Butanoic acid, 3-(phenylmethoxy)-, also known as 3-benzyloxybutanoic acid, is an organic compound with the chemical formula C11H14O3. It is a derivative of butanoic acid, featuring a phenylmethoxy group attached to the third carbon atom. Butanoic acid, 3-(phenylmethoxy)- is a colorless to pale yellow liquid with a molecular weight of 194.23 g/mol. It is soluble in organic solvents and has a melting point of 40-42°C. 3-(phenylmethoxy)-butanoic acid is used in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its versatile chemical structure. It is also known for its potential applications in the fragrance industry and as a building block for the development of new materials.

1135-38-2

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1135-38-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1135-38-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1135-38:
(6*1)+(5*1)+(4*3)+(3*5)+(2*3)+(1*8)=52
52 % 10 = 2
So 1135-38-2 is a valid CAS Registry Number.

1135-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(benzyloxy)butanoic acid

1.2 Other means of identification

Product number -
Other names β-Hydroxybuttersaeure

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:1135-38-2 SDS

1135-38-2Relevant academic research and scientific papers

2-(3,4-DIHYDROXYPHENYL)ETHYL 3-HYDROXYBUTANOATE, COMPOSITION, AND METHOD FOR IMPROVING FUNCTION OF AORTIC ENDOTHELIAL CELL

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Paragraph 0039-0040, (2021/02/19)

The disclosure relates to a compound, 2-(3,4-dihydroxyphenyl)ethyl 3-hydroxybutanoate, for improving aortic endothelial cell function and use thereof. The compound is capable of inhibiting inflammatory response of the human aortic endothelial cells caused by a saturated fatty acid, and preventing an occurrence and progression of atherosclerosis. The compound is capable of reducing human aortic endothelial inflammation caused by a saturated fatty acid, for example, reducing the mRNA levels of interleukin-6 (IL-6), and is capable of effectively protecting the function of mitochondria in human aortic endothelium from being damaged by a saturated fatty acid, for example, increasing the expression of mitochondrial complex I.

3,4-DIHYDROXYPHENETHYL 3-HYDROXYBUTANOATE, PREPARATION AND USE THEREOF

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Paragraph 0101, (2021/03/19)

The present disclosure discloses a novel compound, 3,4-dihydroxyphenethyl 3-hydroxybutanoate, a method for preparing the same and use of the same, and in particular, a compound of formula I, use of the compound of formula I, optically pure isomers of the compound, a mixture of enantiomers in any ratio, or pharmaceutically acceptable salts thereof in preparing health food and drug for relieving brain fatigue, improving learning and memory abilities, and ameliorating mania mood related to brain fatigue.

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