Cas 146335-44-6,3-Cyclohexene-1-carboxylicacid,4-amino-6,6-dimethyl-2-oxo-,methylester

146335-44-6

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Basic information

Product Name: 3-Cyclohexene-1-carboxylicacid,4-amino-6,6-dimethyl-2-oxo-,methylester
Synonyms: 3-Cyclohexene-1-carboxylicacid,4-amino-6,6-dimethyl-2-oxo-,methylester
CAS NO:146335-44-6
Molecular Formula: C10H15NO3
Molecular Weight: 197.23
EINECS: N/A
Product Categories: AMINOACID
Mol File: 146335-44-6.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3-Cyclohexene-1-carboxylicacid,4-amino-6,6-dimethyl-2-oxo-,methylester(CAS DataBase Reference)
NIST Chemistry Reference: 3-Cyclohexene-1-carboxylicacid,4-amino-6,6-dimethyl-2-oxo-,methylester(146335-44-6)
EPA Substance Registry System: 3-Cyclohexene-1-carboxylicacid,4-amino-6,6-dimethyl-2-oxo-,methylester(146335-44-6)

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: 146335-44-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 146335-44-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,3,3 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 146335-44:
(8*1)+(7*4)+(6*6)+(5*3)+(4*3)+(3*5)+(2*4)+(1*4)=126
126 % 10 = 6
So 146335-44-6 is a valid CAS Registry Number.

146335-44-6Upstream product

70328-68-6 methyl 2-hydroxy-6,6-dimethyl-4-oxocyclohex-2-en-1-oate

146335-44-6Downstream Products

146335-44-6Relevant articles and documents

Synthesis of tetra- and pentasubstituted benzenes from dimedone and derivatives

Nelson,Nelson

, p. 1287 - 1290 (2007/10/02)

Treatment of dimedone (5,5-dimethylcyclohexane-1,3-dione) and derivatives with one molar equivalent of sulfuric acid in trifluoroacetic anhydride leads, via sulfonation and a 1,2-methyl group migration, to a variety of dimethylresorcinol derivatives. The

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