Cas 697288-65-6,Carbamic acid, bis(1-methylethyl)-, (1Z,3S,4R)-4-hydroxy-3-methyl-1-phenyl-1-pentenyl ester

697288-65-6

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Basic information

Product Name: Carbamic acid, bis(1-methylethyl)-, (1Z,3S,4R)-4-hydroxy-3-methyl-1-phenyl-1-pentenyl ester
Synonyms:
CAS NO:697288-65-6
Molecular Formula: C19H29NO3
Molecular Weight: 319.444
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: Carbamic acid, bis(1-methylethyl)-, (1Z,3S,4R)-4-hydroxy-3-methyl-1-phenyl-1-pentenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, bis(1-methylethyl)-, (1Z,3S,4R)-4-hydroxy-3-methyl-1-phenyl-1-pentenyl ester(697288-65-6)
EPA Substance Registry System: Carbamic acid, bis(1-methylethyl)-, (1Z,3S,4R)-4-hydroxy-3-methyl-1-phenyl-1-pentenyl ester(697288-65-6)

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: 697288-65-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 697288-65-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,7,2,8 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 697288-65:
(8*6)+(7*9)+(6*7)+(5*2)+(4*8)+(3*8)+(2*6)+(1*5)=236
236 % 10 = 6
So 697288-65-6 is a valid CAS Registry Number.

697288-65-6Upstream product

75-07-0 acetaldehyde

697288-65-6Downstream Products

697288-65-6Relevant academic research and scientific papers

Enantio- and diastereoselective synthesis of highly substituted acylcyclopropanes from homoaldol products by stereospecific homoallylic cyclization

Kalkofen, Rainer,Brandau, Sven,Uenaldi, Seda,Frohlich, Roland,Hoppe, Dieter

, p. 4571 - 4580 (2005)

Highly enantioenriched 4-hydroxy-1-alkenyl N,N-diisopropylcarbamates, easily available by asymmetric homoaldol reaction, cyclize by treatment with sodium hydride to form (1r,2t,3t)-configured 1-acylcyclopropanes with high diastereoselectivity. The decisiv

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