Cas 688359-70-8,(1S,5S,6S,1'R)-6-hydroxy-6-(1-phenylethyl-aminomethyl)-bicyclo[3.3.0]octan-2-one ethylene ketal

688359-70-8

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Basic information

Product Name: (1S,5S,6S,1'R)-6-hydroxy-6-(1-phenylethyl-aminomethyl)-bicyclo[3.3.0]octan-2-one ethylene ketal
Synonyms: (1S,5S,6S,1'R)-6-hydroxy-6-(1-phenylethyl-aminomethyl)-bicyclo[3.3.0]octan-2-one ethylene ketal
CAS NO:688359-70-8
Molecular Formula:
Molecular Weight: 317.428
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: (1S,5S,6S,1'R)-6-hydroxy-6-(1-phenylethyl-aminomethyl)-bicyclo[3.3.0]octan-2-one ethylene ketal(CAS DataBase Reference)
NIST Chemistry Reference: (1S,5S,6S,1'R)-6-hydroxy-6-(1-phenylethyl-aminomethyl)-bicyclo[3.3.0]octan-2-one ethylene ketal(688359-70-8)
EPA Substance Registry System: (1S,5S,6S,1'R)-6-hydroxy-6-(1-phenylethyl-aminomethyl)-bicyclo[3.3.0]octan-2-one ethylene ketal(688359-70-8)

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: 688359-70-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 688359-70-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,8,3,5 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 688359-70:
(8*6)+(7*8)+(6*8)+(5*3)+(4*5)+(3*9)+(2*7)+(1*0)=228
228 % 10 = 8
So 688359-70-8 is a valid CAS Registry Number.

688359-70-8Upstream product

688359-70-8Downstream Products

688359-70-8Relevant academic research and scientific papers

New β-amino alcohols with a bicyclo[3.3.0]octane scaffold in an asymmetric Henry reaction

Zhong, Yu-Wu,Tian, Ping,Lin, Guo-Qiang

, p. 771 - 776 (2007/10/03)

A new category of β-amino alcohols with a bicyclo[3.3.0]octane scaffold has been synthesized and used in the direct asymmetric nitroaldol reaction (Henry reaction). Up to 74% ee was obtained with the addition of nitromethane to relatively bulky aldehydes.

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