Cas 161659-06-9,(S)-3-Benzyloxycarbonylamino-N-[(1S,2R)-2-hydroxy-1-methyl-3-((1S,2S,4R)-1,3,3-trimethyl-bicyclo[2.2.1]hept-2-yl)-propyl]-succinamic acid benzyl ester

161659-06-9

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Basic information

Product Name: (S)-3-Benzyloxycarbonylamino-N-[(1S,2R)-2-hydroxy-1-methyl-3-((1S,2S,4R)-1,3,3-trimethyl-bicyclo[2.2.1]hept-2-yl)-propyl]-succinamic acid benzyl ester
Synonyms: (S)-3-Benzyloxycarbonylamino-N-[(1S,2R)-2-hydroxy-1-methyl-3-((1S,2S,4R)-1,3,3-trimethyl-bicyclo[2.2.1]hept-2-yl)-propyl]-succinamic acid benzyl ester
CAS NO:161659-06-9
Molecular Formula:
Molecular Weight: 564.722
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: (S)-3-Benzyloxycarbonylamino-N-[(1S,2R)-2-hydroxy-1-methyl-3-((1S,2S,4R)-1,3,3-trimethyl-bicyclo[2.2.1]hept-2-yl)-propyl]-succinamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-Benzyloxycarbonylamino-N-[(1S,2R)-2-hydroxy-1-methyl-3-((1S,2S,4R)-1,3,3-trimethyl-bicyclo[2.2.1]hept-2-yl)-propyl]-succinamic acid benzyl ester(161659-06-9)
EPA Substance Registry System: (S)-3-Benzyloxycarbonylamino-N-[(1S,2R)-2-hydroxy-1-methyl-3-((1S,2S,4R)-1,3,3-trimethyl-bicyclo[2.2.1]hept-2-yl)-propyl]-succinamic acid benzyl ester(161659-06-9)

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: 161659-06-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 161659-06-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,6,5 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 161659-06:
(8*1)+(7*6)+(6*1)+(5*6)+(4*5)+(3*9)+(2*0)+(1*6)=139
139 % 10 = 9
So 161659-06-9 is a valid CAS Registry Number.

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161659-06-9Relevant academic research and scientific papers

The sweetness and stereochemistry of L-aspartyl-fenchylaminoalcohol derivatives

Yuasa, Yoshifumi,Nagakura, Akira,Tsuruta, Haruki

, p. 6891 - 6894 (1994)

Four fenchylaminoalcohols were derived from (+)-fenchone in five steps. They were resolved with (+)- and (-)-tartaric acid, then condensed with N-carbobenzoxy-L-aspartic acid β-benzylester followed by hydrogenolysis to give four L-aspartyl-fenchylaminoalc

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