Cas 1155765-82-4,(R)-diphenyl (6-methyl-2-pyridylsulfonylamino)phenylmethylphosphonate

1155765-82-4

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Basic information

Product Name: (R)-diphenyl (6-methyl-2-pyridylsulfonylamino)phenylmethylphosphonate
Synonyms: (R)-diphenyl (6-methyl-2-pyridylsulfonylamino)phenylmethylphosphonate
CAS NO:1155765-82-4
Molecular Formula:
Molecular Weight: 494.508
EINECS: N/A
Product Categories: N/A
Mol File: 1155765-82-4.mol
Article Data: 1

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: (R)-diphenyl (6-methyl-2-pyridylsulfonylamino)phenylmethylphosphonate(CAS DataBase Reference)
NIST Chemistry Reference: (R)-diphenyl (6-methyl-2-pyridylsulfonylamino)phenylmethylphosphonate(1155765-82-4)
EPA Substance Registry System: (R)-diphenyl (6-methyl-2-pyridylsulfonylamino)phenylmethylphosphonate(1155765-82-4)

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: 1155765-82-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1155765-82-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,5,7,6 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1155765-82:
(9*1)+(8*1)+(7*5)+(6*5)+(5*7)+(4*6)+(3*5)+(2*8)+(1*2)=174
174 % 10 = 4
So 1155765-82-4 is a valid CAS Registry Number.

1155765-82-4Upstream product

1155765-82-4Downstream Products

1155765-82-4Relevant articles and documents

Organocatalytic enantioselective hydrophosphonylation of sulfonylimines having a heteroarenesulfonyl group as a novel stereocontroller

Nakamura, Shuichi,Nakashima, Hiroki,Yamamura, Akiko,Shibata, Norio,Torua, Takeshi

scheme or table, p. 1209 - 1212 (2009/06/17)

Organocatalytic enantioselective hydrophosphonylation of imines having the a heteroarenesulfonyl group afforded the respective products with high enantioselectivity. Both enantiomers of α-amino phosphonates were obtained by using different Cinchona alkalo

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