Cas 347885-29-4,(4S,5R,2'S,3'R)-1,5-dimethyl-4-phenyl-3-[(2'-N-acetylaziridinyl-3'-isopropyl)carbonyl]-imidazolidin-2-one

347885-29-4

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Basic information

Product Name: (4S,5R,2'S,3'R)-1,5-dimethyl-4-phenyl-3-[(2'-N-acetylaziridinyl-3'-isopropyl)carbonyl]-imidazolidin-2-one
Synonyms: (4S,5R,2'S,3'R)-1,5-dimethyl-4-phenyl-3-[(2'-N-acetylaziridinyl-3'-isopropyl)carbonyl]-imidazolidin-2-one
CAS NO:347885-29-4
Molecular Formula:
Molecular Weight: 343.426
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: (4S,5R,2'S,3'R)-1,5-dimethyl-4-phenyl-3-[(2'-N-acetylaziridinyl-3'-isopropyl)carbonyl]-imidazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (4S,5R,2'S,3'R)-1,5-dimethyl-4-phenyl-3-[(2'-N-acetylaziridinyl-3'-isopropyl)carbonyl]-imidazolidin-2-one(347885-29-4)
EPA Substance Registry System: (4S,5R,2'S,3'R)-1,5-dimethyl-4-phenyl-3-[(2'-N-acetylaziridinyl-3'-isopropyl)carbonyl]-imidazolidin-2-one(347885-29-4)

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: 347885-29-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 347885-29-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,7,8,8 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 347885-29:
(8*3)+(7*4)+(6*7)+(5*8)+(4*8)+(3*5)+(2*2)+(1*9)=194
194 % 10 = 4
So 347885-29-4 is a valid CAS Registry Number.

347885-29-4Upstream product

347885-29-4Downstream Products

347885-30-7 (4S,5R,4'S,5'R)-4,5-dihydro-2-methyl-4-[(1',5'-dimethyl-4'-phenylimidazolidin-2'-on-3'-yl)carbonyl]-5-isopropyloxazole

347885-29-4Relevant academic research and scientific papers

Asymmetric synthesis of 5-isopropyl-oxazoline-4-imide as syn-hydroxyleucine precursor

Cardillo, Giuliana,Gentilucci, Luca,Gianotti, Massimo,Tolomelli, Alessandra

, p. 563 - 569 (2007/10/03)

The synthesis of syn N-acetyl-hydroxyleucinemethyl ester is reported through the ring expansion of aziridine-2-imides to oxazoline-4-imides. The key steps of the synthesis are the 1,4-addition of O-benzylhydroxylamine to unsaturated imides, promoted by Le

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