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Benzoic acid, 4-amino-2,3,5-trifluoro-, methyl ester (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 138724-32-0 Structure
  • Basic information

    1. Product Name: Benzoic acid, 4-amino-2,3,5-trifluoro-, methyl ester (9CI)
    2. Synonyms: Benzoic acid, 4-amino-2,3,5-trifluoro-, methyl ester (9CI)
    3. CAS NO:138724-32-0
    4. Molecular Formula: C8H6F3NO2
    5. Molecular Weight: 205.1339496
    6. EINECS: N/A
    7. Product Categories: AMINOACID
    8. Mol File: 138724-32-0.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: Benzoic acid, 4-amino-2,3,5-trifluoro-, methyl ester (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid, 4-amino-2,3,5-trifluoro-, methyl ester (9CI)(138724-32-0)
    11. EPA Substance Registry System: Benzoic acid, 4-amino-2,3,5-trifluoro-, methyl ester (9CI)(138724-32-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 138724-32-0(Hazardous Substances Data)

138724-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138724-32-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,7,2 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 138724-32:
(8*1)+(7*3)+(6*8)+(5*7)+(4*2)+(3*4)+(2*3)+(1*2)=140
140 % 10 = 0
So 138724-32-0 is a valid CAS Registry Number.

138724-32-0SDS

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 methyl 4-amino-2,3,5-trifluorobenzoate

1.2 Other means of identification

Product number -
Other names 4-Amino-2,3,5-trifluoro-benzoic acid methyl ester

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:138724-32-0 SDS

138724-32-0Relevant articles and documents

FUSED TRICYCLIC COMPOUNDS USEFUL AS ANTICANCER AGENTS

-

Page/Page column 33; 111, (2020/09/19)

The specification relates to compounds of Formula (A) and pharmaceutically acceptable salts thereof. The specification also relates to processes and intermediates used for their preparation, pharmaceutical compositions containing them and their use in the treatment of cell proliferative disorders.

Photocatalytic hydrodefluorination: Facile access to partially fluorinated aromatics

Senaweera, Sameera M.,Singh, Anuradha,Weaver, Jimmie D.

, p. 3002 - 3005 (2014/03/21)

Polyfluorinated aromatics are essential to materials science as well as the pharmaceutical and agrochemical industries and yet are often difficult to access. This Communication describes a photocatalytic hydrodefluorination approach which begins with easily accessible perfluoroarenes and selectively reduces the C-F bonds. The method allows facile access to a number of partially fluorinated arenes and takes place with unprecedented catalytic activity using a safe and inexpensive amine as the reductant.

Toward the Development of Radiolabeled Fluorophenyl Azide-Based Photolabeling Reagents: Synthesis and Photolysis of Iodinated 4-Azidoperfluorobenzoates and 4-Azido-3,5,6-trifluorobenzoates

Cai, Sui Xiong,Glenn, Dennis J.,Keana, John F. W.

, p. 1299 - 1304 (2007/10/02)

Two approaches for the incorporation of iodine into funtionalized perfluorophenyl azides (PFPAs) were demonstrated by the synthesis of 3, 5, and 8, with the azido and iodo groups in the same aryl ring, and 14 and 15, with the azido and iodo groups in diff

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