Cas 127703-67-7,1-[4-Amino-5-(1-amino-ethyl)-2-hydroxy-2-methyl-6-phenyl-cyclohexyl]-ethanone

127703-67-7

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Basic information

Product Name: 1-[4-Amino-5-(1-amino-ethyl)-2-hydroxy-2-methyl-6-phenyl-cyclohexyl]-ethanone
Synonyms: 1-[4-Amino-5-(1-amino-ethyl)-2-hydroxy-2-methyl-6-phenyl-cyclohexyl]-ethanone
CAS NO:127703-67-7
Molecular Formula:
Molecular Weight: 290.406
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: 1-[4-Amino-5-(1-amino-ethyl)-2-hydroxy-2-methyl-6-phenyl-cyclohexyl]-ethanone(CAS DataBase Reference)
NIST Chemistry Reference: 1-[4-Amino-5-(1-amino-ethyl)-2-hydroxy-2-methyl-6-phenyl-cyclohexyl]-ethanone(127703-67-7)
EPA Substance Registry System: 1-[4-Amino-5-(1-amino-ethyl)-2-hydroxy-2-methyl-6-phenyl-cyclohexyl]-ethanone(127703-67-7)

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: 127703-67-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 127703-67-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,7,0 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 127703-67:
(8*1)+(7*2)+(6*7)+(5*7)+(4*0)+(3*3)+(2*6)+(1*7)=127
127 % 10 = 7
So 127703-67-7 is a valid CAS Registry Number.

127703-67-7Upstream product

100483-82-7 2,4-diacetyl-3-phenyl-5-hydroxy-5-methylcyclohexanone

127703-67-7Downstream Products

127703-67-7Relevant academic research and scientific papers

NATURE OF THE TRANSFORMATIONS OF POLYSUBSTITUTED 3-HYDROXYCYCLOHEXANONES UNDER THE CONDITIONS OF CATALYTIC HYDROGENATION AND HYDROAMINATION

Kharchenko, V. G.,Smirnova, N. S.,Rybina, G. I.

, p. 2286 - 2289 (2007/10/02)

Substituted 3-hydroxycyclohexanones were converted by reduction and hydroamination into the corresponding 1,3-cyclohexanediols and 3-aminocyclohexanols.The carbonyl group in the acetyl substituent at position 6 of cyclohexanones (Ic, d) is highly reactive

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