Cas 463300-58-5,2-[isobutyl-(4-methoxy-benzenesulfonyl)-amino]-4-phenylmethanesulfonyl-butyric acid methyl ester

463300-58-5

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Basic information

Product Name: 2-[isobutyl-(4-methoxy-benzenesulfonyl)-amino]-4-phenylmethanesulfonyl-butyric acid methyl ester
Synonyms: 2-[isobutyl-(4-methoxy-benzenesulfonyl)-amino]-4-phenylmethanesulfonyl-butyric acid methyl ester
CAS NO:463300-58-5
Molecular Formula:
Molecular Weight: 497.634
EINECS: N/A
Product Categories: N/A

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-[isobutyl-(4-methoxy-benzenesulfonyl)-amino]-4-phenylmethanesulfonyl-butyric acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[isobutyl-(4-methoxy-benzenesulfonyl)-amino]-4-phenylmethanesulfonyl-butyric acid methyl ester(463300-58-5)
EPA Substance Registry System: 2-[isobutyl-(4-methoxy-benzenesulfonyl)-amino]-4-phenylmethanesulfonyl-butyric acid methyl ester(463300-58-5)

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: 463300-58-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 463300-58-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,3,3,0 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 463300-58:
(8*4)+(7*6)+(6*3)+(5*3)+(4*0)+(3*0)+(2*5)+(1*8)=125
125 % 10 = 5
So 463300-58-5 is a valid CAS Registry Number.

463300-58-5Upstream product

463300-58-5Downstream Products

463300-58-5Relevant academic research and scientific papers

N-aryl sulfonyl homocysteine hydroxamate inhibitors of matrix metalloproteinases: Further probing of the S1, S1′, and S2′ pockets

Hanessian,Moitessier,Gauchet,Viau

, p. 3066 - 3073 (2007/10/03)

A series of N-arylsulfonyl S-alkyl homocysteine hydroxamic acids were synthesized with variations in three subsites corresponding to P1, P1′, and P2′. Enzyme assays with a variety of MMPs revealed activity at the low nanomolar level.

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