Cas 103841-76-5,(2R,3R)-3-Methyl-oxirane-2-carboxylic acid (4-methoxy-benzyl)-(3-phenylsulfanyl-prop-2-ynyl)-amide

103841-76-5

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Basic information

Product Name: (2R,3R)-3-Methyl-oxirane-2-carboxylic acid (4-methoxy-benzyl)-(3-phenylsulfanyl-prop-2-ynyl)-amide
Synonyms: (2R,3R)-3-Methyl-oxirane-2-carboxylic acid (4-methoxy-benzyl)-(3-phenylsulfanyl-prop-2-ynyl)-amide
CAS NO:103841-76-5
Molecular Formula:
Molecular Weight: 367.469
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,3R)-3-Methyl-oxirane-2-carboxylic acid (4-methoxy-benzyl)-(3-phenylsulfanyl-prop-2-ynyl)-amide(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R)-3-Methyl-oxirane-2-carboxylic acid (4-methoxy-benzyl)-(3-phenylsulfanyl-prop-2-ynyl)-amide(103841-76-5)
EPA Substance Registry System: (2R,3R)-3-Methyl-oxirane-2-carboxylic acid (4-methoxy-benzyl)-(3-phenylsulfanyl-prop-2-ynyl)-amide(103841-76-5)

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: 103841-76-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 103841-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,8,4 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 103841-76:
(8*1)+(7*0)+(6*3)+(5*8)+(4*4)+(3*1)+(2*7)+(1*6)=105
105 % 10 = 5
So 103841-76-5 is a valid CAS Registry Number.

103841-76-5Upstream product

103841-76-5Downstream Products

98729-69-2 (3S,4S)-1-(p-methoxybenzyl)-3-<(R)-1-hydroxyethyl>-4-phenylthioethynyl-2-azetidinone

103841-76-5Relevant academic research and scientific papers

CYCLIZATION REACTION OF N-PROPARGYL EPOXYAMIDE TO ACETYLENIC 2-AZETIDINONE, A PRECURSOR TO THIENAMYCIN AND RELATED CARBAPENEMS

Marayuma, Hiroshi,Shiozaki, Masao,Oida, Sadao,Hiraoka, Tetsuo

, p. 4521 - 4522 (2007/10/02)

Base treatment of N-propargyl epoxyamide 5 afforded the acetylenic 3-(hydroxyethyl)-2-azetidinone 9a, which was subsequently transformed to phenyl thiolester 2, a versatile intermediate for the carbapenem synthesis.

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