Cas 229032-22-8,(S)-{2-[2-(2,2-dimethyl-5-oxo-[1,3]dioxolan-4-yl)-acetyl]-4-hydroxy-phenyl}-carbamic acid tert-butyl ester

229032-22-8

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Basic information

Product Name: (S)-{2-[2-(2,2-dimethyl-5-oxo-[1,3]dioxolan-4-yl)-acetyl]-4-hydroxy-phenyl}-carbamic acid tert-butyl ester
Synonyms: (S)-{2-[2-(2,2-dimethyl-5-oxo-[1,3]dioxolan-4-yl)-acetyl]-4-hydroxy-phenyl}-carbamic acid tert-butyl ester
CAS NO:229032-22-8
Molecular Formula:
Molecular Weight: 365.383
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)-{2-[2-(2,2-dimethyl-5-oxo-[1,3]dioxolan-4-yl)-acetyl]-4-hydroxy-phenyl}-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-{2-[2-(2,2-dimethyl-5-oxo-[1,3]dioxolan-4-yl)-acetyl]-4-hydroxy-phenyl}-carbamic acid tert-butyl ester(229032-22-8)
EPA Substance Registry System: (S)-{2-[2-(2,2-dimethyl-5-oxo-[1,3]dioxolan-4-yl)-acetyl]-4-hydroxy-phenyl}-carbamic acid tert-butyl ester(229032-22-8)

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: 229032-22-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 229032-22-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,9,0,3 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 229032-22:
(8*2)+(7*2)+(6*9)+(5*0)+(4*3)+(3*2)+(2*2)+(1*2)=108
108 % 10 = 8
So 229032-22-8 is a valid CAS Registry Number.

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229032-22-8Relevant academic research and scientific papers

Practical synthesis of blepharismone, a mating inducing pheromone of Blepharisma japonicum

Takihiro, Hisashi,Uruma, Yoshiyuki,Usuki, Yoshinosuke,Miyake, Akio,Iio, Hideo

, p. 2339 - 2343 (2007/10/03)

Both enantiomers of blepharismone, a mating inducing pheromone produced by type II cells of Blepharisma japonicum, were synthesized via the Stille cross-coupling reaction of [4-(tert-butyl-dimethyl-silanyloxy)-2-trimethylstannanyl-phenyl]-carbamic acid te

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