Cas 105601-84-1,(3R,4R)-4-<(1-methyl-1H-tetrazol-5-yl)thio>-1-(1-methoxycarbonyl-2-methylprop-1-enyl)-3-phenylacetamido-2-azetidinone

105601-84-1

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Basic information

Product Name: (3R,4R)-4-<(1-methyl-1H-tetrazol-5-yl)thio>-1-(1-methoxycarbonyl-2-methylprop-1-enyl)-3-phenylacetamido-2-azetidinone
Synonyms:
CAS NO:105601-84-1
Molecular Formula:
Molecular Weight: 430.487
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: (3R,4R)-4-<(1-methyl-1H-tetrazol-5-yl)thio>-1-(1-methoxycarbonyl-2-methylprop-1-enyl)-3-phenylacetamido-2-azetidinone(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4R)-4-<(1-methyl-1H-tetrazol-5-yl)thio>-1-(1-methoxycarbonyl-2-methylprop-1-enyl)-3-phenylacetamido-2-azetidinone(105601-84-1)
EPA Substance Registry System: (3R,4R)-4-<(1-methyl-1H-tetrazol-5-yl)thio>-1-(1-methoxycarbonyl-2-methylprop-1-enyl)-3-phenylacetamido-2-azetidinone(105601-84-1)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 105601-84-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 105601-84-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,6,0 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 105601-84:
(8*1)+(7*0)+(6*5)+(5*6)+(4*0)+(3*1)+(2*8)+(1*4)=91
91 % 10 = 1
So 105601-84-1 is a valid CAS Registry Number.

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105601-84-1Relevant academic research and scientific papers

Synthesis of 4-Substituted Monocyclic &β-Lactams by a Lewis Acid-mediated Reaction

Yoshida, Chosaku,Hori, Takako,Momonoi, Kaishu,Tanaka, Kiyoshi,Kishimoto, Sumiko,Saikawa, Isamu

, p. 839 - 846 (2007/10/02)

The synthesis of 4-substituted monocyclic β-lactam is described.The key step in this method was accomplished by nucleophilic replacement in the presence of Lewis acid, that is, (3S,4S)-4-acetoxy-3-phenylacetamido-2-azetidinone derivatives or oxazolinoazet

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