Cas 1258323-53-3,2-hydroxy-N-(2-oxo-2-(2-oxotetrahydrothiophen-3-ylamino)ethyl)benzamide

1258323-53-3

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Basic information

Product Name: 2-hydroxy-N-(2-oxo-2-(2-oxotetrahydrothiophen-3-ylamino)ethyl)benzamide
Synonyms: 2-hydroxy-N-(2-oxo-2-(2-oxotetrahydrothiophen-3-ylamino)ethyl)benzamide
CAS NO:1258323-53-3
Molecular Formula:
Molecular Weight: 294.331
EINECS: N/A
Product Categories: N/A
Mol File: 1258323-53-3.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-hydroxy-N-(2-oxo-2-(2-oxotetrahydrothiophen-3-ylamino)ethyl)benzamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-hydroxy-N-(2-oxo-2-(2-oxotetrahydrothiophen-3-ylamino)ethyl)benzamide(1258323-53-3)
EPA Substance Registry System: 2-hydroxy-N-(2-oxo-2-(2-oxotetrahydrothiophen-3-ylamino)ethyl)benzamide(1258323-53-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1258323-53-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1258323-53-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,3,2 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1258323-53:
(9*1)+(8*2)+(7*5)+(6*8)+(5*3)+(4*2)+(3*3)+(2*5)+(1*3)=153
153 % 10 = 3
So 1258323-53-3 is a valid CAS Registry Number.

1258323-53-3Upstream product

1258323-53-3Downstream Products

1258323-53-3Relevant articles and documents

2-HYDROXYHIPPURIC ACID ANALOGS, AND METHODS FOR THEIR SYNTHESIS AND USE

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Paragraph 0090; 0091, (2013/04/13)

The present invention relates to novel 2-hydroxyhippuric acid analogs, and methods for their synthesis and use. Such analogs are designed to provide a protected or functional moiety such as a free thiol (-SH) group or a protected thiol group, thereby providing a convenient linkage chemistry for coupling under mild conditions to a suitable group on a target protein, polypeptide, solid phase or detectable label.

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