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3-(3-Hydroxy-phenyl)-2-methyl-acrylic acid, also known as 3-(3-hydroxyphenyl)-2-methylprop-2-enoic acid, is an organic compound with the chemical formula C10H10O3. It is a derivative of acrylic acid, featuring a phenyl ring with a hydroxyl group at the para position and a methyl group at the alpha position. 3-(3-HYDROXY-PHENYL)-2-METHYL-ACRYLIC ACID is characterized by its aromatic structure and conjugated double bonds, which contribute to its chemical reactivity and potential applications in various fields, such as pharmaceuticals, materials science, and as a precursor in the synthesis of other organic compounds.

6317-50-6

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6317-50-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6317-50-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6317-50:
(6*6)+(5*3)+(4*1)+(3*7)+(2*5)+(1*0)=86
86 % 10 = 6
So 6317-50-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O3/c1-7(10(12)13)5-8-3-2-4-9(11)6-8/h2-6,11H,1H3,(H,12,13)/b7-5-

6317-50-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3-hydroxyphenyl)-2-methylprop-2-enoic 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

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More Details:6317-50-6 SDS

6317-50-6Relevant academic research and scientific papers

Synthesis of Albicidin Derivatives: Assessing the Role of N-terminal Acylation on the Antibacterial Activity

Kerwat, Dennis,Gr?tz, Stefan,Kretz, Julian,Seidel, Maria,Kunert, Maria,Weston, John B.,Süssmuth, Roderich D.

supporting information, p. 1899 - 1903 (2016/10/12)

The peptide antibiotic albicidin, which is synthesized by the plant pathogenic bacterium, Xanthomonas albilineans, represents the most prominent member of a new class of antibacterial gyrase inhibitors. It shows remarkable antibacterial activities against Gram-positive and Gram-negative microorganisms. Its unique structure potentially represents a new lead structure for the development of an antibacterial drug. Here we report the synthesis of 14 albicidin derivatives with structural variations at the N-terminus, primarily investigating the effects of variation of cinnamoyl, phenylpropanoyl, and benzoyl residues. Gyrase inhibition in vitro and determination of minimal inhibitory concentrations were assessed in parallel. Activities in a nanomolar range and the importance of N-acylation were demonstrated.

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