Cas 200055-82-9,Carbamic acid, (3-oxo-1-cyclopenten-1-yl)-, 1,1-dimethylethyl ester (9CI)

200055-82-9

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Basic information

Product Name: Carbamic acid, (3-oxo-1-cyclopenten-1-yl)-, 1,1-dimethylethyl ester (9CI)
Synonyms: Carbamic acid, (3-oxo-1-cyclopenten-1-yl)-, 1,1-dimethylethyl ester (9CI)
CAS NO:200055-82-9
Molecular Formula: C10H15NO3
Molecular Weight: 197.231
EINECS: N/A
Product Categories: N-BOC
Mol File: 200055-82-9.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: 281.9±40.0 °C(Predicted)
Flash Point: N/A
Appearance: /
Density: 1.11±0.1 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
PKA: 10.46±0.20(Predicted)
CAS DataBase Reference: Carbamic acid, (3-oxo-1-cyclopenten-1-yl)-, 1,1-dimethylethyl ester (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, (3-oxo-1-cyclopenten-1-yl)-, 1,1-dimethylethyl ester (9CI)(200055-82-9)
EPA Substance Registry System: Carbamic acid, (3-oxo-1-cyclopenten-1-yl)-, 1,1-dimethylethyl ester (9CI)(200055-82-9)

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: 200055-82-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 200055-82-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,0,5 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 200055-82:
(8*2)+(7*0)+(6*0)+(5*0)+(4*5)+(3*5)+(2*8)+(1*2)=69
69 % 10 = 9
So 200055-82-9 is a valid CAS Registry Number.

200055-82-9Upstream product

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200055-82-9Relevant articles and documents

Enantioselective allene/enone photocycloadditions: The use of an inexpensive optically active 1,3-disubstituted allene

Shepard, Mary S.,Carreira, Erick M.

, p. 16253 - 16276 (2007/10/03)

We report the preparation and use of an inexpensive readily prepared optically active 1,3-disubstituted allene that may be utilized for enantioselective intramolecular allene/enone photocycloadditions. In addition, we describe novel substrates for intramo

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