Cas 873441-97-5,(2S)-2-(N-p-toluene-sulphonyl)-amino-1-tert-butyldiphenylsilyloxy-4-diazo-6-methoxy-hexan-3-one

873441-97-5

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Basic information

Product Name: (2S)-2-(N-p-toluene-sulphonyl)-amino-1-tert-butyldiphenylsilyloxy-4-diazo-6-methoxy-hexan-3-one
Synonyms: (2S)-2-(N-p-toluene-sulphonyl)-amino-1-tert-butyldiphenylsilyloxy-4-diazo-6-methoxy-hexan-3-one
CAS NO:873441-97-5
Molecular Formula:
Molecular Weight: 579.792
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: (2S)-2-(N-p-toluene-sulphonyl)-amino-1-tert-butyldiphenylsilyloxy-4-diazo-6-methoxy-hexan-3-one(CAS DataBase Reference)
NIST Chemistry Reference: (2S)-2-(N-p-toluene-sulphonyl)-amino-1-tert-butyldiphenylsilyloxy-4-diazo-6-methoxy-hexan-3-one(873441-97-5)
EPA Substance Registry System: (2S)-2-(N-p-toluene-sulphonyl)-amino-1-tert-butyldiphenylsilyloxy-4-diazo-6-methoxy-hexan-3-one(873441-97-5)

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: 873441-97-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 873441-97-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,4,4 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 873441-97:
(8*8)+(7*7)+(6*3)+(5*4)+(4*4)+(3*1)+(2*9)+(1*7)=195
195 % 10 = 5
So 873441-97-5 is a valid CAS Registry Number.

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873441-97-5Relevant academic research and scientific papers

Asymmetric synthesis of cis-2,4-disubstituted azetidin-3-ones from metal carbene chemistry

Burtoloso, Antonio Carlos B.,Correia, Carlos Roque D.

, p. 5636 - 5646 (2007/10/03)

Several chiral cis-2,4-disubstituted azetidin-3-ones were prepared as single diastereoisomers from N-protected amino acids, employing a highly stereoselective copper carbenoid N-H insertion reaction of diazoketones. These azetidin-3-ones were then convert

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