Cas 89556-78-5,1-Pyrrolidinesulfonamide, N-[(2-chloro-5-nitrophenyl)methylene]-2-(methoxymethyl)-, (S)-

89556-78-5

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Basic information

Product Name: 1-Pyrrolidinesulfonamide, N-[(2-chloro-5-nitrophenyl)methylene]-2-(methoxymethyl)-, (S)-
Synonyms:
CAS NO:89556-78-5
Molecular Formula: C13H16ClN3O5S
Molecular Weight: 361.806
EINECS: N/A
Product Categories: N/A
Mol File: 89556-78-5.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: 1-Pyrrolidinesulfonamide, N-[(2-chloro-5-nitrophenyl)methylene]-2-(methoxymethyl)-, (S)-(CAS DataBase Reference)
NIST Chemistry Reference: 1-Pyrrolidinesulfonamide, N-[(2-chloro-5-nitrophenyl)methylene]-2-(methoxymethyl)-, (S)-(89556-78-5)
EPA Substance Registry System: 1-Pyrrolidinesulfonamide, N-[(2-chloro-5-nitrophenyl)methylene]-2-(methoxymethyl)-, (S)-(89556-78-5)

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: 89556-78-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 89556-78-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,5 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89556-78:
(7*8)+(6*9)+(5*5)+(4*5)+(3*6)+(2*7)+(1*8)=195
195 % 10 = 5
So 89556-78-5 is a valid CAS Registry Number.

89556-78-5Upstream product

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89556-78-5Relevant articles and documents

Chiral Sulfamides: Synthesis of Optically Active 2-Sulfamyloxaziridines. High Enantioselectivity in the Asymmetric Oxidation of Sulfides to Sulfoxides

Davis, Franklin A.,McCauley, John P.,Harakal, Mark E.

, p. 1465 - 1467 (2007/10/02)

The first synthesis of optically active 2-sulfamyloxaziridines 4a-d and 5a-d, which affords high enantioselectivity (38-68 percent ee) for asymmetric oxidations of sulfides to sulfoxides, is described.

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