Cas 1229422-29-0,2-(3-methyl-4-nitroisoxazol-5-yl)-1-(4-nitrophenyl)ethanesulfonic acid

1229422-29-0

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Basic information

Product Name: 2-(3-methyl-4-nitroisoxazol-5-yl)-1-(4-nitrophenyl)ethanesulfonic acid
Synonyms: 2-(3-methyl-4-nitroisoxazol-5-yl)-1-(4-nitrophenyl)ethanesulfonic acid
CAS NO:1229422-29-0
Molecular Formula:
Molecular Weight: 357.301
EINECS: N/A
Product Categories: N/A
Mol File: 1229422-29-0.mol
Article Data: 2

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-nitroisoxazol-5-yl)-1-(4-nitrophenyl)ethanesulfonic acid(CAS DataBase Reference)
NIST Chemistry Reference: 2-(3-methyl-4-nitroisoxazol-5-yl)-1-(4-nitrophenyl)ethanesulfonic acid(1229422-29-0)
EPA Substance Registry System: 2-(3-methyl-4-nitroisoxazol-5-yl)-1-(4-nitrophenyl)ethanesulfonic acid(1229422-29-0)

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: 1229422-29-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1229422-29-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,9,4,2 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1229422-29:
(9*1)+(8*2)+(7*2)+(6*9)+(5*4)+(4*2)+(3*2)+(2*2)+(1*9)=140
140 % 10 = 0
So 1229422-29-0 is a valid CAS Registry Number.

1229422-29-0Upstream product

78080-53-2 3-Methyl-4-nitro-5-[(E)-2-(4-nitro-phenyl)-vinyl]-isoxazole

1229422-29-0Downstream Products

1229422-29-0Relevant articles and documents

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

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

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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