Cas 127802-55-5,Diisopropyl-carbamic acid (Z)-(3S,4S)-4-hydroxy-1,3-dimethyl-4-phenyl-pent-1-enyl ester

127802-55-5

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Basic information

Product Name: Diisopropyl-carbamic acid (Z)-(3S,4S)-4-hydroxy-1,3-dimethyl-4-phenyl-pent-1-enyl ester
Synonyms:
CAS NO:127802-55-5
Molecular Formula:
Molecular Weight: 333.471
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: Diisopropyl-carbamic acid (Z)-(3S,4S)-4-hydroxy-1,3-dimethyl-4-phenyl-pent-1-enyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Diisopropyl-carbamic acid (Z)-(3S,4S)-4-hydroxy-1,3-dimethyl-4-phenyl-pent-1-enyl ester(127802-55-5)
EPA Substance Registry System: Diisopropyl-carbamic acid (Z)-(3S,4S)-4-hydroxy-1,3-dimethyl-4-phenyl-pent-1-enyl ester(127802-55-5)

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: 127802-55-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 127802-55-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,8,0 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 127802-55:
(8*1)+(7*2)+(6*7)+(5*8)+(4*0)+(3*2)+(2*5)+(1*5)=125
125 % 10 = 5
So 127802-55-5 is a valid CAS Registry Number.

127802-55-5Upstream product

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127802-55-5Relevant academic research and scientific papers

Enantiomerically enriched allylstannanes from chiral allyllithium derivatives and their highly regio-, diastereo- and enantioselective hydroxyalkylation

Kramer,Schwark,Hoppe

, p. 7037 - 7040 (2007/10/02)

Chiral, non-racemic 1-lithio-2-alkenyl carbamates, generated by stereospecific deprotonation, are stannylated in a syn-S(E), reaction. The optically active allylstannanes thus obtained, undergo enantioselective homoaldol addition under the influence of TiCl4.

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