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Benzoic acid, 6-amino-2-methyl-3-nitro-, 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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  • 132734-42-0 Structure
  • Basic information

    1. Product Name: Benzoic acid, 6-amino-2-methyl-3-nitro-, methyl ester (9CI)
    2. Synonyms: Benzoic acid, 6-amino-2-methyl-3-nitro-, methyl ester (9CI);6-amino-2-methyl-3-nitro-benzoic acid methyl ester
    3. CAS NO:132734-42-0
    4. Molecular Formula: C9H10N2O4
    5. Molecular Weight: 210.1867
    6. EINECS: N/A
    7. Product Categories: AMINOACID
    8. Mol File: 132734-42-0.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, 6-amino-2-methyl-3-nitro-, methyl ester (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid, 6-amino-2-methyl-3-nitro-, methyl ester (9CI)(132734-42-0)
    11. EPA Substance Registry System: Benzoic acid, 6-amino-2-methyl-3-nitro-, methyl ester (9CI)(132734-42-0)
  • 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: 132734-42-0(Hazardous Substances Data)

132734-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132734-42-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,7,3 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 132734-42:
(8*1)+(7*3)+(6*2)+(5*7)+(4*3)+(3*4)+(2*4)+(1*2)=110
110 % 10 = 0
So 132734-42-0 is a valid CAS Registry Number.

132734-42-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-amino-2-methyl-3-nitro-benzoic acid methyl ester

1.2 Other means of identification

Product number -
Other names methyl 2-methyl-3-nitro-6-aminobenzoate

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:132734-42-0 SDS

132734-42-0Downstream Products

132734-42-0Relevant articles and documents

Preparation of saccharincarboxylic acids and -carboxylic acid esters

-

, (2008/06/13)

Saccharincarboxylic acids and -carboxylic acid esters of the formula I STR1 where the substituents have the following meanings: L and M are hydrogen, alkyl, alkoxy, alkylthio, chlorine, cyano, alkylsulfonyl, nitro or trifluoromethyl; Z is hydrogen, alkyl, cycloalkyl, alkyl, aryl or aralkyl; R is H or C1 -C6 -alkyl, are prepared by reacting corresponding bromo- or iodo-substituted saccharin derivatives of the formula II STR2 where L, M and Z have the abovementioned meanings, or if Z≠H, compounds of the formula III STR3 in the presence of a palladium, nickel, cobalt or rhodium transition metal catalyst and of a base with carbon monoxide and water or a C1 -C6 -alcohol under elevated pressure.

Saccharin derivatives

-

, (2008/06/13)

Saccharin derivatives of the formula I STR1 where the substituents have the following meanings: L and M are hydrogen, C1 -C4 -alkyl, C1 -C4 -alkoxy, C1 -C4 -alkylthio, chlorine, cyano, meth

5-hydroxypyrazol-4-ylcarbonyl-substituted saccharin derivatives

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, (2008/06/13)

5-Hydroxypyrazol-4-ylcarbonyl-substituted saccharin derivatives of the formula I STR1 where the substituents have the following meanings: L and M are hydrogen, C1 -C4 -alkyl, C1 -C4 -alkoxy, C1 -Csub

Saccharin derivatives

-

, (2008/06/13)

Saccharin derivatives of the formula I STR1 where the substituents have the following meanings: L and M are hydrogen, C1 -C4 -alkyl, C1 -C4 -alkoxy, C1 -C4 -alkylthio, chlorine, cyano, methylsulfonyl, nitro or trifluoromethyl; Z is hydrogen, C1 -C4 -alkyl, C3 -C8 -cycloalkyl, C3 -C6 -alkenyl, C3 -C5 -alkynyl, C1 -C4 -acyl, benzyl or phenyl, the phenyl rings in each case being unsubstituted or substituted by halogen or C1 -C4 -alkyl; Q is a radical T-J, where T is a carbonyl radical CO or the radical --CHY, J is a 4-linked isoxazole ring of the formula II STR2 where R1 is hydrogen or C1 -C4 -alkyl and R2 is C1 -C4 -alkyl, cyclopropyl, 1-methylcyclopropyl or 1-methylthiocyclopropyl; Y is an OH group, a hydroxyl group which may be acylated by C2 -C4 -acyl or a chlorine atom; and agriculturally customary salts of the compounds I are described.

Saccharin derivatives

-

, (2008/06/13)

Saccharin derivatives of the formula I STR1 where the substituents have the following meanings: L and M are hydrogen, alkyl, alkoxy, alkylthio, chlorine, cyano, methylsulfonyl, nitro or trifluoromethyl; Z is hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl,

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