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100960-33-6

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100960-33-6 Usage

Chemical compound

2-Amino-6-chlorobenzoic acid, hydrochloride

Properties

Benzoic acid derivative
Contains an amino group and a chloro substituent attached to the benzene ring
Pharmaceutical intermediate
Hydrochloride salt form for increased solubility in water
Potential as a corrosion inhibitor
Building block in organic synthesis

Specific content

Used in synthesis of various drugs, including antiviral and antitumor agents
Increased solubility in water for drug formulation and delivery
Potential as a corrosion inhibitor
Building block in organic synthesis for manufacturing new chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 100960-33-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,9,6 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 100960-33:
(8*1)+(7*0)+(6*0)+(5*9)+(4*6)+(3*0)+(2*3)+(1*3)=86
86 % 10 = 6
So 100960-33-6 is a valid CAS Registry Number.

100960-33-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-6-chlorobenzoic acid hydrochloride

1.2 Other means of identification

Product number -
Other names 5-Chloroanthranillic acid hydrochloride

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:100960-33-6 SDS

100960-33-6Relevant articles and documents

Herbicidal substituted benzoylsulfonamides

-

, (2008/06/13)

Compound of the formula STR1 in which A is O, S, or NR3 ; G is CH or N; R and R1 are independently alkyl, alkoxy, haloalkoxy or alkylamino; R2 is phenyl, substituted phenyl, alkyl, cycloalkyl, haloalkyl or --CH2 [(R4)C(R5)n --Z; R3 and R7 are, independently, hydrogen, alkyl, --C(O)NH2 or --C(O)alkyl; R4 and R5 are independently hydrogen, alkyl, or halogen; R6 is halogen, alkyl, alkoxy, haloalkoxy, NO2, amino, alkyl substituted amino, or acyl substituted amino; n is 0 to 5; Z is cyano, amino, alkylamino, dialkylamino, --NHCO2 alkyl, alkoxy, alkylthio, alkylsulfonyl, alkenyl, alkynyl, phenyl or substituted phenyl; and Q is hydrogen, halogen, alkyl, alkoxy, haloalkoxy, nitro, amino, haloalkyl, alkythio, alkylsulfonyl, phenyl, substituted phenyl or phenoxy; or a 5 or 6 membered aromatic heterocycle having the formula STR2 in which "m" is 0 or 1; A' is O, S, or NR7 ; and X, X', Y, Y', W, W', V, V', U and Z' are independently N, O, S, --CH-- or --CR6. Intermediates for preparation of the benzoylsulfonamides are also disclosed.

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