Cas 1202006-41-4,(1R,2R,4S)-1-methyl-4-(prop-1-en-2-yl)cyclohexane-1,2-diamine

1202006-41-4

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Basic information

Product Name: (1R,2R,4S)-1-methyl-4-(prop-1-en-2-yl)cyclohexane-1,2-diamine
Synonyms: (1R,2R,4S)-1-methyl-4-(prop-1-en-2-yl)cyclohexane-1,2-diamine
CAS NO:1202006-41-4
Molecular Formula:
Molecular Weight: 168.282
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: (1R,2R,4S)-1-methyl-4-(prop-1-en-2-yl)cyclohexane-1,2-diamine(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R,4S)-1-methyl-4-(prop-1-en-2-yl)cyclohexane-1,2-diamine(1202006-41-4)
EPA Substance Registry System: (1R,2R,4S)-1-methyl-4-(prop-1-en-2-yl)cyclohexane-1,2-diamine(1202006-41-4)

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: 1202006-41-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1202006-41-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,2,0,0 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1202006-41:
(9*1)+(8*2)+(7*0)+(6*2)+(5*0)+(4*0)+(3*6)+(2*4)+(1*1)=64
64 % 10 = 4
So 1202006-41-4 is a valid CAS Registry Number.

1202006-41-4Upstream product

1202006-41-4Downstream Products

1202006-48-1 C₂₂H₄₆N₂O₆P₂

1202006-41-4Relevant academic research and scientific papers

A convenient synthesis of new diamine, amino alcohol and aminophosphines chiral auxiliaries based on limonene oxide

Cimarelli, Cristina,Fratoni, Davide,Palmieri, Gianni

experimental part, p. 2234 - 2239 (2010/03/03)

A strategy for the synthesis of new chiral auxiliaries based upon vicinal diamines, amino alcohols and aminophosphines, obtained from limonene oxide, has been developed. The methodology allows the preparation of (1R,2R,4S)-1-methyl-4-(prop-1-en-2-yl)cyclo

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