Cas 863012-04-8,(3aR,5S,7R,7aS)-7-Benzyloxymethyl-5-phenoxy-2-trichloromethyl-3a,4,7,7a-tetrahydro-1,6-dioxa-3-aza-5-phospha-indene 5-oxide

863012-04-8

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Basic information

Product Name: (3aR,5S,7R,7aS)-7-Benzyloxymethyl-5-phenoxy-2-trichloromethyl-3a,4,7,7a-tetrahydro-1,6-dioxa-3-aza-5-phospha-indene 5-oxide
Synonyms: (3aR,5S,7R,7aS)-7-Benzyloxymethyl-5-phenoxy-2-trichloromethyl-3a,4,7,7a-tetrahydro-1,6-dioxa-3-aza-5-phospha-indene 5-oxide
CAS NO:863012-04-8
Molecular Formula:
Molecular Weight: 490.707
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: (3aR,5S,7R,7aS)-7-Benzyloxymethyl-5-phenoxy-2-trichloromethyl-3a,4,7,7a-tetrahydro-1,6-dioxa-3-aza-5-phospha-indene 5-oxide(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,5S,7R,7aS)-7-Benzyloxymethyl-5-phenoxy-2-trichloromethyl-3a,4,7,7a-tetrahydro-1,6-dioxa-3-aza-5-phospha-indene 5-oxide(863012-04-8)
EPA Substance Registry System: (3aR,5S,7R,7aS)-7-Benzyloxymethyl-5-phenoxy-2-trichloromethyl-3a,4,7,7a-tetrahydro-1,6-dioxa-3-aza-5-phospha-indene 5-oxide(863012-04-8)

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: 863012-04-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 863012-04-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,0,1 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 863012-04:
(8*8)+(7*6)+(6*3)+(5*0)+(4*1)+(3*2)+(2*0)+(1*4)=138
138 % 10 = 8
So 863012-04-8 is a valid CAS Registry Number.

863012-04-8Upstream product

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863012-04-8Relevant academic research and scientific papers

P-heterocyclic building blocks: Application to the stereoselective synthesis of P-sugars

Stoianova, Diana S.,Whitehead, Alan,Hanson, Paul R.

, p. 5880 - 5889 (2007/10/03)

A strategy relying on the utilization of stereoselective additions to allyldiphenylphosphonate esters and subsequent ring-closing metathesis (RCM) to access P-chiral P-heterocyclic building blocks for the synthesis of phosphono sugars is described. These

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