Cas 1041464-61-2,4-(4-(2-hydroxypropan-2-yl)-1H-1,2,3-triazol-1-yl)benzenesulfonamide

1041464-61-2

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Basic information

Product Name: 4-(4-(2-hydroxypropan-2-yl)-1H-1,2,3-triazol-1-yl)benzenesulfonamide
Synonyms: 4-(4-(2-hydroxypropan-2-yl)-1H-1,2,3-triazol-1-yl)benzenesulfonamide
CAS NO:1041464-61-2
Molecular Formula:
Molecular Weight: 282.323
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: 4-(4-(2-hydroxypropan-2-yl)-1H-1,2,3-triazol-1-yl)benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-(4-(2-hydroxypropan-2-yl)-1H-1,2,3-triazol-1-yl)benzenesulfonamide(1041464-61-2)
EPA Substance Registry System: 4-(4-(2-hydroxypropan-2-yl)-1H-1,2,3-triazol-1-yl)benzenesulfonamide(1041464-61-2)

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: 1041464-61-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1041464-61-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,1,4,6 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1041464-61:
(9*1)+(8*0)+(7*4)+(6*1)+(5*4)+(4*6)+(3*4)+(2*6)+(1*1)=112
112 % 10 = 2
So 1041464-61-2 is a valid CAS Registry Number.

1041464-61-2Upstream product

1041464-61-2Downstream Products

1041464-62-3 4-(4-(2-hydroxypropan-2-yl)-1H-1,2,3-triazol-1-yl)benzenesulfonyl azide

1041464-61-2Relevant academic research and scientific papers

Efficient synthesis of sulfonyl azides from sulfonamides

Raushel, Jessica,Pitram, Suresh M.,Fokin, Valery V.

, p. 3385 - 3388 (2008)

(Equation Presented) Triflyl azide serves as an efficient diazo transfer reagent in this first direct synthesis of sulfonyl azides from readily available and stable sulfonamides. The process is experimentally simple, mild, and high-yielding. Sulfonyl azid

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