Cas 126280-02-2,2-butyl-5,5-dimethyl-3-methoxy-4-methoxycarbonyl-2-cyclohexen-1-one

126280-02-2

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Basic information

Product Name: 2-butyl-5,5-dimethyl-3-methoxy-4-methoxycarbonyl-2-cyclohexen-1-one
Synonyms: 2-butyl-5,5-dimethyl-3-methoxy-4-methoxycarbonyl-2-cyclohexen-1-one
CAS NO:126280-02-2
Molecular Formula:
Molecular Weight: 268.353
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-butyl-5,5-dimethyl-3-methoxy-4-methoxycarbonyl-2-cyclohexen-1-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-butyl-5,5-dimethyl-3-methoxy-4-methoxycarbonyl-2-cyclohexen-1-one(126280-02-2)
EPA Substance Registry System: 2-butyl-5,5-dimethyl-3-methoxy-4-methoxycarbonyl-2-cyclohexen-1-one(126280-02-2)

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: 126280-02-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 126280-02-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,2,8 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 126280-02:
(8*1)+(7*2)+(6*6)+(5*2)+(4*8)+(3*0)+(2*0)+(1*2)=102
102 % 10 = 2
So 126280-02-2 is a valid CAS Registry Number.

126280-02-2Upstream product

118082-05-6 2-butyryl-3-methoxy-4-methoxycarbonyl-5,5-dimethylcyclohex-2-en-1-one

126280-02-2Downstream Products

126280-02-2Relevant academic research and scientific papers

IONIC HYDROGENATION OF ENOLIC DERIVATIVES OF CYCLOHEXANE β-TRIKETONES

Lakhvich, F. A.,Lis, L. G.,Rubinov, D. B.,Rubinova, I. L.,Akhrem, A. A.

, p. 1493 - 1498 (2007/10/02)

The ionic hydrogenation of the enolic derivatives (enamines, enol ethers, vinyl chloride) of 2-butyryl-5,5-dimethyl-1,3-cyclohexanedione and its 4-methoxycarbonyl-substituted analog takes place regiospecifically with reduction of the keto group in the acy

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