Cas 474974-00-0,(2R,3S)-2-Isobutyl-3-(2-oxo-oxazolidine-3-carbonyl)-hex-5-enoic acid ((S)-1-methylcarbamoyl-2-phenyl-ethyl)-amide

474974-00-0

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Basic information

Product Name: (2R,3S)-2-Isobutyl-3-(2-oxo-oxazolidine-3-carbonyl)-hex-5-enoic acid ((S)-1-methylcarbamoyl-2-phenyl-ethyl)-amide
Synonyms: (2R,3S)-2-Isobutyl-3-(2-oxo-oxazolidine-3-carbonyl)-hex-5-enoic acid ((S)-1-methylcarbamoyl-2-phenyl-ethyl)-amide
CAS NO:474974-00-0
Molecular Formula:
Molecular Weight: 443.543
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: (2R,3S)-2-Isobutyl-3-(2-oxo-oxazolidine-3-carbonyl)-hex-5-enoic acid ((S)-1-methylcarbamoyl-2-phenyl-ethyl)-amide(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S)-2-Isobutyl-3-(2-oxo-oxazolidine-3-carbonyl)-hex-5-enoic acid ((S)-1-methylcarbamoyl-2-phenyl-ethyl)-amide(474974-00-0)
EPA Substance Registry System: (2R,3S)-2-Isobutyl-3-(2-oxo-oxazolidine-3-carbonyl)-hex-5-enoic acid ((S)-1-methylcarbamoyl-2-phenyl-ethyl)-amide(474974-00-0)

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: 474974-00-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 474974-00-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,4,9,7 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 474974-00:
(8*4)+(7*7)+(6*4)+(5*9)+(4*7)+(3*4)+(2*0)+(1*0)=190
190 % 10 = 0
So 474974-00-0 is a valid CAS Registry Number.

474974-00-0Upstream product

35373-92-3 L-phenylalanine methylamide

474974-00-0Downstream Products

474974-03-3 2-allyl-3-isobutyl-N⁴-(1-methylcarbamoyl-2-phenyl-ethyl)-N¹-(tetrahydro-pyran-2-yloxy)-succinamide

474974-00-0Relevant academic research and scientific papers

An efficient method for synthesis of succinate-based MMP inhibitors

Sibi, Mukund P.,Hasegawa, Hikaru

, p. 3347 - 3349 (2002)

(matrix presented) A differentially protected fumarate undergoes radical addition followed by allylstannane trapping to provide disubstituted succinates in good yields and high anti diastereoselectivity. The conversion of the succinate to a known MMP inhi

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