Cas 113525-95-4,Carbamic acid, [2-oxo-1-(phenylmethoxy)-4-(2-propenyl)-3-azetidinyl]-, 1,1-dimethylethyl ester, trans-

113525-95-4

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Basic information

Product Name: Carbamic acid, [2-oxo-1-(phenylmethoxy)-4-(2-propenyl)-3-azetidinyl]-, 1,1-dimethylethyl ester, trans-
Synonyms:
CAS NO:113525-95-4
Molecular Formula: C18H24N2O4
Molecular Weight: 332.4
EINECS: N/A
Product Categories: N/A
Mol File: 113525-95-4.mol

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, [2-oxo-1-(phenylmethoxy)-4-(2-propenyl)-3-azetidinyl]-, 1,1-dimethylethyl ester, trans-(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [2-oxo-1-(phenylmethoxy)-4-(2-propenyl)-3-azetidinyl]-, 1,1-dimethylethyl ester, trans-(113525-95-4)
EPA Substance Registry System: Carbamic acid, [2-oxo-1-(phenylmethoxy)-4-(2-propenyl)-3-azetidinyl]-, 1,1-dimethylethyl ester, trans-(113525-95-4)

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: 113525-95-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 113525-95-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,5,2 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 113525-95:
(8*1)+(7*1)+(6*3)+(5*5)+(4*2)+(3*5)+(2*9)+(1*5)=104
104 % 10 = 4
So 113525-95-4 is a valid CAS Registry Number.

113525-95-4Upstream product

113525-95-4Downstream Products

113525-95-4Relevant academic research and scientific papers

MILD AND SELECTIVE RING-CLEAVAGE OF CYCLIC CARBAMATES TO AMINO ALCOHOLS

Ishizuka, Tadao,Kunieda, Takehisa

, p. 4185 - 4188 (1987)

N-tert-Butoxycarbonylated 2-oxazolidinones and tetrahydro-2-oxazinones are smoothly cleaved to acyclic N-Boc-amino alcohols on treatment with catalytic amounts of cesium carbonate at room temperature.The versatility of the procedure is demonstrated in a facile cleavage of highly functionalized heterocycles without epimerization and β-elimination.

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