Cas 528869-41-2,(Z)-(4-hydroxy-6-phenyl-hex-1-enyl)-(4-methoxy-phenyl)-carbamic acid tert-butyl ester

528869-41-2

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Basic information

Product Name: (Z)-(4-hydroxy-6-phenyl-hex-1-enyl)-(4-methoxy-phenyl)-carbamic acid tert-butyl ester
Synonyms: (Z)-(4-hydroxy-6-phenyl-hex-1-enyl)-(4-methoxy-phenyl)-carbamic acid tert-butyl ester
CAS NO:528869-41-2
Molecular Formula:
Molecular Weight: 397.514
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: (Z)-(4-hydroxy-6-phenyl-hex-1-enyl)-(4-methoxy-phenyl)-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-(4-hydroxy-6-phenyl-hex-1-enyl)-(4-methoxy-phenyl)-carbamic acid tert-butyl ester(528869-41-2)
EPA Substance Registry System: (Z)-(4-hydroxy-6-phenyl-hex-1-enyl)-(4-methoxy-phenyl)-carbamic acid tert-butyl ester(528869-41-2)

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: 528869-41-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 528869-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,8,8,6 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 528869-41:
(8*5)+(7*2)+(6*8)+(5*8)+(4*6)+(3*9)+(2*4)+(1*1)=202
202 % 10 = 2
So 528869-41-2 is a valid CAS Registry Number.

528869-41-2Upstream product

528869-41-2Downstream Products

528869-41-2Relevant academic research and scientific papers

Cyclopropane structural units from homoaldol adducts

Taylor, Richard E.,Risatti, Christina A.,Engelhardt, F. Conrad,Schmitt, Michael J.

, p. 1377 - 1379 (2003)

(Matrix presented) An efficient two-step homologation of aldehydes to cyclopropylaldehydes has been developed. Activation of homoaldol adducts derived from O-enecarbamates and N-enecarbamates provided high yields of cyclopropylaldehydes with good to excel

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