Cas 953805-47-5,Naphthalene-1-sulfonic acid ((1S,2S)-2-amino-cyclohexyl)-amide

953805-47-5

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Basic information

Product Name: Naphthalene-1-sulfonic acid ((1S,2S)-2-amino-cyclohexyl)-amide
Synonyms: Naphthalene-1-sulfonic acid ((1S,2S)-2-amino-cyclohexyl)-amide
CAS NO:953805-47-5
Molecular Formula:
Molecular Weight: 304.413
EINECS: N/A
Product Categories: N/A
Mol File: 953805-47-5.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: Naphthalene-1-sulfonic acid ((1S,2S)-2-amino-cyclohexyl)-amide(CAS DataBase Reference)
NIST Chemistry Reference: Naphthalene-1-sulfonic acid ((1S,2S)-2-amino-cyclohexyl)-amide(953805-47-5)
EPA Substance Registry System: Naphthalene-1-sulfonic acid ((1S,2S)-2-amino-cyclohexyl)-amide(953805-47-5)

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: 953805-47-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 953805-47-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,3,8,0 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 953805-47:
(8*9)+(7*5)+(6*3)+(5*8)+(4*0)+(3*5)+(2*4)+(1*7)=195
195 % 10 = 5
So 953805-47-5 is a valid CAS Registry Number.

953805-47-5Upstream product

953805-47-5Downstream Products

953805-47-5Relevant articles and documents

Synthesis of chiral sulfonamide/Schiff base ligands

Balsells, Jaume,Mejorado, Lupe,Phillips, Mimi,Ortega, Fernando,Aguirre, Gerardo,Somanathan, Ratnasamy,Walsh, Patrick J.

, p. 4135 - 4142 (1998)

We report a facile two step synthesis of chiral ligands for bonding to transition metals. The ligands are easily prepared from trans, 1,2- diaminocyclohexane by reaction with sulfonyl chlorides to give amino- sulfonamide compounds. These intermediates are

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