Cas 1373702-75-0,(1S,5R,6S)-5-azido-6-hydroxycyclohex-2-en-1-yl 4-nitrobenzoate

1373702-75-0

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Basic information

Product Name: (1S,5R,6S)-5-azido-6-hydroxycyclohex-2-en-1-yl 4-nitrobenzoate
Synonyms: (1S,5R,6S)-5-azido-6-hydroxycyclohex-2-en-1-yl 4-nitrobenzoate
CAS NO:1373702-75-0
Molecular Formula:
Molecular Weight: 304.262
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: (1S,5R,6S)-5-azido-6-hydroxycyclohex-2-en-1-yl 4-nitrobenzoate(CAS DataBase Reference)
NIST Chemistry Reference: (1S,5R,6S)-5-azido-6-hydroxycyclohex-2-en-1-yl 4-nitrobenzoate(1373702-75-0)
EPA Substance Registry System: (1S,5R,6S)-5-azido-6-hydroxycyclohex-2-en-1-yl 4-nitrobenzoate(1373702-75-0)

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: 1373702-75-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1373702-75-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,7,0 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1373702-75:
(9*1)+(8*3)+(7*7)+(6*3)+(5*7)+(4*0)+(3*2)+(2*7)+(1*5)=160
160 % 10 = 0
So 1373702-75-0 is a valid CAS Registry Number.

1373702-75-0Upstream product

1174522-50-9 (3S,4S,5S)-3-(4-nitro)benzoyloxy-4,5-epoxycyclohex-1-ene

1373702-75-0Downstream Products

1373702-75-0Relevant academic research and scientific papers

Formal synthesis of tamiflu: Conversion of tamiflu into tamiphosphor

Gunasekera, Dinara S.

, p. 573 - 576 (2012)

A short, enantiomeric, synthesis of Shibasakis 3rd generation intermediate to form (-)-oseltamivir phosphate (Tamiflu) has been achieved in eight steps with the use of inexpensive starting materials. A formal synthetic route to convert tamiflu into tamiphosphor via Fangs tamiphosphor intermediate has been accomplished. Georg Thieme Verlag Stuttgart · New York.

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