Cas 136814-33-0,dimethyl 2-(3-chlorophenyl)-6-hydroxy-4-(2-hydroxyethylamino)-6-methylcyclohex-3-en-1,3-dicarboxylate

136814-33-0

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Basic information

Product Name: dimethyl 2-(3-chlorophenyl)-6-hydroxy-4-(2-hydroxyethylamino)-6-methylcyclohex-3-en-1,3-dicarboxylate
Synonyms: dimethyl 2-(3-chlorophenyl)-6-hydroxy-4-(2-hydroxyethylamino)-6-methylcyclohex-3-en-1,3-dicarboxylate
CAS NO:136814-33-0
Molecular Formula:
Molecular Weight: 397.856
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: dimethyl 2-(3-chlorophenyl)-6-hydroxy-4-(2-hydroxyethylamino)-6-methylcyclohex-3-en-1,3-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: dimethyl 2-(3-chlorophenyl)-6-hydroxy-4-(2-hydroxyethylamino)-6-methylcyclohex-3-en-1,3-dicarboxylate(136814-33-0)
EPA Substance Registry System: dimethyl 2-(3-chlorophenyl)-6-hydroxy-4-(2-hydroxyethylamino)-6-methylcyclohex-3-en-1,3-dicarboxylate(136814-33-0)

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: 136814-33-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 136814-33-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,8,1 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 136814-33:
(8*1)+(7*3)+(6*6)+(5*8)+(4*1)+(3*4)+(2*3)+(1*3)=130
130 % 10 = 0
So 136814-33-0 is a valid CAS Registry Number.

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136814-33-0Relevant academic research and scientific papers

2,3,8,8a-Tetrahydro-7H-oxazolo[3,2-a]pyridine: A new heterocyclic system

Feliciano, Arturo San,Caballero, Esther,Pereira, Juan A. P.,Puebla, Pilar

, p. 6503 - 6510 (2007/10/02)

Compounds with the previously unreported skeleton of 2,3,8,8a-tetrahydro-7H-oxazolo [3,2-a]pyridine were prepared by reactions between α,β-unsaturated ketones or aldehydes and N-hydroxyethyl-enamines of acetoacetate esters. Other compounds like 1,4-dihydropyridines, aminocyclohexene and cyclohexadiene derivatives were also formed as minor products.

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