Cas 70142-91-5,(4R)-4α-[(R)-3-Hydroxybutyl]-5β-hydroxymethyl-3,3-dimethylcyclohexanone

70142-91-5

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Basic information

Product Name: (4R)-4α-[(R)-3-Hydroxybutyl]-5β-hydroxymethyl-3,3-dimethylcyclohexanone
Synonyms: (4R)-4α-[(R)-3-Hydroxybutyl]-5β-hydroxymethyl-3,3-dimethylcyclohexanone;Nigakialcohol
CAS NO:70142-91-5
Molecular Formula: C₁₃H₂₄O₃
Molecular Weight: 228.32786
EINECS: N/A
Product Categories: N/A
Mol File: 70142-91-5.mol

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: (4R)-4α-[(R)-3-Hydroxybutyl]-5β-hydroxymethyl-3,3-dimethylcyclohexanone(CAS DataBase Reference)
NIST Chemistry Reference: (4R)-4α-[(R)-3-Hydroxybutyl]-5β-hydroxymethyl-3,3-dimethylcyclohexanone(70142-91-5)
EPA Substance Registry System: (4R)-4α-[(R)-3-Hydroxybutyl]-5β-hydroxymethyl-3,3-dimethylcyclohexanone(70142-91-5)

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: 70142-91-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 70142-91-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,1,4 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 70142-91:
(7*7)+(6*0)+(5*1)+(4*4)+(3*2)+(2*9)+(1*1)=95
95 % 10 = 5
So 70142-91-5 is a valid CAS Registry Number.

70142-91-5Upstream product

128533-22-2 (1S,4R,5S)-4-((R)-3-Hydroxy-butyl)-5-hydroxymethyl-3,3-dimethyl-cyclohexanol

70142-91-5Downstream Products

70143-12-3 Deoxonigaki-Alkohol

70142-91-5Relevant academic research and scientific papers

The structures of two new ionone glucosides from melia toosendan and a novel type of selective bio-oxidation

Nakanishi,Konishi,Murata,Inada,Fujii,Tanaka,Fajiwara

, p. 830 - 832 (2007/10/02)

The structures of two new ionone glucosides, melia-ionosides A and B, isolated from leaves of Melia toosendan were determined based on the combined evidence of chemical, spectral, and X-ray studies. In addition, a novel type of selective bio-oxidation was

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