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succinimido (1,5-naphthyridin-3-yl)formate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53512-20-2

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53512-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53512-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,1 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53512-20:
(7*5)+(6*3)+(5*5)+(4*1)+(3*2)+(2*2)+(1*0)=92
92 % 10 = 2
So 53512-20-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H9N3O5/c17-9-3-4-10(18)16(9)21-13(20)7-6-15-8-2-1-5-14-11(8)12(7)19/h1-2,5-6H,3-4H2,(H,15,19)

53512-20-2SDS

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 (4-oxo-3,4-dihydro-[1,5]naphthyridine-3-carbonyloxy)-succinimide

1.2 Other means of identification

Product number -
Other names succinimido (1,5-naphthyridin-3-yl)formate

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:53512-20-2 SDS

53512-20-2Downstream Products

53512-20-2Relevant academic research and scientific papers

Penicillins substituted with heterocyclic and substituted phenyl groups

-

, (2008/06/13)

Novel penicillins of the formula SPC1 Wherein EQU1 represents a substituted or unsubstituted benzene or nitrogen atom-containing heteroaromatic ring which may be substituted, EQU2 represents a pyridine, pyrazine or pyridazine ring, X represents an oxygen or sulfur atom, Y represents a hydrogen atom or a loer alkoxycarbonyl or lower alkanoyl group, and R1, R2 and R3 are each a hydrogen or halogen atom or a nitro, lower alkylamino, di(lower)alkylamino, aine, lower alkoxycarbonylamino, lower alkanoylamino, amino(lower)alkyl, lower alkyl, lower alkoxy, hydroxyl, sulfamoyl, trifluoromethyl, lower alkylthio or lower alkylsulfonyl group, excluding the cases where all of R1, R2 and R3 are hydrogen atoms and where R1 is a hydroxyl group and R2 and R3 are each a hydrogen or halogen atom, and their nontoxic, pharmaceutically acceptable salts, which can be prepared by reacting a carboxylic acid of the formula: EQU3 wherein EQU4 X and Y are each as defined above or its reactive derivative with a compound of the formula: SPC2 Wherein R1, R2 and R3 are each as defined above or its reactive derivative, and are ueful as antimicrobial agents against gram-positive and gram-negative bacteria including Pseudomonas.

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