Cas 1262968-92-2,2-(3-methyl-4-nitro-isoxazol-5-yl)-1-p-tolylethanesulfonic acid

1262968-92-2

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Basic information

Product Name: 2-(3-methyl-4-nitro-isoxazol-5-yl)-1-p-tolylethanesulfonic acid
Synonyms: 2-(3-methyl-4-nitro-isoxazol-5-yl)-1-p-tolylethanesulfonic acid
CAS NO:1262968-92-2
Molecular Formula:
Molecular Weight: 326.33
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: 2-(3-methyl-4-nitro-isoxazol-5-yl)-1-p-tolylethanesulfonic acid(CAS DataBase Reference)
NIST Chemistry Reference: 2-(3-methyl-4-nitro-isoxazol-5-yl)-1-p-tolylethanesulfonic acid(1262968-92-2)
EPA Substance Registry System: 2-(3-methyl-4-nitro-isoxazol-5-yl)-1-p-tolylethanesulfonic acid(1262968-92-2)

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: 1262968-92-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1262968-92-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,9,6 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1262968-92:
(9*1)+(8*2)+(7*6)+(6*2)+(5*9)+(4*6)+(3*8)+(2*9)+(1*2)=192
192 % 10 = 2
So 1262968-92-2 is a valid CAS Registry Number.

1262968-92-2Upstream product

75143-79-2 3-methyl-4-nitro-5-(4-methylstyryl)isoxazole

1262968-92-2Downstream Products

1262968-92-2Relevant academic research and scientific papers

Development of a mild procedure for the addition of bisulfite to electrophilic olefins

Fini, Francesco,Nagabelli, Murali,Adamo, Mauro F. A.

supporting information; experimental part, p. 3163 - 3168 (2011/02/22)

The sulfonylation of activated alkenes is an important yet unexplored reaction due to the harshness of conditions required. We have identified a procedure which allowed the reaction of alkenes with equimolar amounts of bisulfite at room temperature. Copyr

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