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AKOS B029957 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 104483-15-0 Structure
  • Basic information

    1. Product Name: AKOS B029957
    2. Synonyms: AKOS B029957;2-Methyl-3-thiophen-2-yl-propionic acid;2-methyl-3-(thiophen-2-yl)propanoic acid
    3. CAS NO:104483-15-0
    4. Molecular Formula: C8H10O2S
    5. Molecular Weight: 170.2288
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104483-15-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: AKOS B029957(CAS DataBase Reference)
    10. NIST Chemistry Reference: AKOS B029957(104483-15-0)
    11. EPA Substance Registry System: AKOS B029957(104483-15-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 104483-15-0(Hazardous Substances Data)

104483-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104483-15-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,4,8 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 104483-15:
(8*1)+(7*0)+(6*4)+(5*4)+(4*8)+(3*3)+(2*1)+(1*5)=100
100 % 10 = 0
So 104483-15-0 is a valid CAS Registry Number.

104483-15-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name α-methyl-2-thiophenepropanoic acid

1.2 Other means of identification

Product number -
Other names 2-methyl-3-[2]thienyl-propionic acid

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:104483-15-0 SDS

104483-15-0Downstream Products

104483-15-0Relevant articles and documents

Microbial deracemization of α-substituted carboxylic acids: Control of the reaction path

Kato, Dai-Ichiro,Miyamoto, Kenji,Ohta, Hiromichi

, p. 2965 - 2973 (2007/10/03)

A novel approach to preparing optically active α-substituted carboxylic acids using the whole cells of Nocardia diaphanozonaria JCM 3208 is described. When 2-phenylthiopropanoic acid and 2-methyl-3-phenylpropanoic acid were subjected to the reaction under aerobic conditions, the oxidation reaction proceeded preferentially rather than deracemization of these substrates. Herein, we report the design of reaction conditions to increase the deracemization activity in preference to oxidation reactions. In addition, we have successfully detected a metabolic intermediate in the reaction mixture of 2-methyl-3-phenylpropanoic acid, which indicates that the deracemization is a competitive reaction against the α-oxidation pathway of fatty acid metabolism.

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