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3H-Phenoxazine-1,9-dicarboxamide, 2-amino-6-chloro-N1-(3-(dimethylamin o)propyl)-4-methyl-3-oxo-, monohydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81325-75-9

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81325-75-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81325-75-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,2 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 81325-75:
(7*8)+(6*1)+(5*3)+(4*2)+(3*5)+(2*7)+(1*5)=119
119 % 10 = 9
So 81325-75-9 is a valid CAS Registry Number.
InChI:InChI=1/C20H22ClN5O4.ClH/c1-9-16(27)13(22)12(20(29)24-7-4-8-26(2)3)15-17(9)30-18-11(21)6-5-10(19(23)28)14(18)25-15;/h5-6H,4,7-8,22H2,1-3H3,(H2,23,28)(H,24,29);1H

81325-75-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-6-chloro-1-N-[3-(dimethylamino)propyl]-4-methyl-3-oxophenoxazine-1,9-dicarboxamide,hydrochloride

1.2 Other means of identification

Product number -
Other names 2-Amino-6-chloro-N1-(3-(dimethylamino)propyl)-4-methyl-3-oxo-3H-phenoxazine-1,9-dicarboxamide monohydrochloride

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:81325-75-9 SDS

81325-75-9Downstream Products

81325-75-9Relevant academic research and scientific papers

SYNTHESIS OF ACTINOMYCIN ANALOGS XIII. UNSYMMETRICAL DERIVATIVES OF CINNABARIC ACID

Tsukerman, B. V.,Glibin, E. N.,Ginzburg, O. F.

, p. 1503 - 1508 (2007/10/02)

During the oxidation of mixtures of substituted 2-amino-3-hydroxy-4-methylbenzamides with the ester or amide of 2-amino-3-hydroxy-4-chlorobenzoic acid the formation of the 2-amino-4,6-dimethyl-3H-3-oxophenoxazine derivative is suppressed by the increase i

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