Cas 124754-67-2,2H-1,3-Oxazin-2-one,6-ethenyltetrahydro-4-(1-methylethyl)-,cis-(9CI)

124754-67-2

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Basic information

Product Name: 2H-1,3-Oxazin-2-one,6-ethenyltetrahydro-4-(1-methylethyl)-,cis-(9CI)
Synonyms: 2H-1,3-Oxazin-2-one,6-ethenyltetrahydro-4-(1-methylethyl)-,cis-(9CI)
CAS NO:124754-67-2
Molecular Formula: C9H15NO2
Molecular Weight: 169.22
EINECS: N/A
Product Categories: ISOPROPYL
Mol File: 124754-67-2.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2H-1,3-Oxazin-2-one,6-ethenyltetrahydro-4-(1-methylethyl)-,cis-(9CI)(CAS DataBase Reference)
NIST Chemistry Reference: 2H-1,3-Oxazin-2-one,6-ethenyltetrahydro-4-(1-methylethyl)-,cis-(9CI)(124754-67-2)
EPA Substance Registry System: 2H-1,3-Oxazin-2-one,6-ethenyltetrahydro-4-(1-methylethyl)-,cis-(9CI)(124754-67-2)

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: 124754-67-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 124754-67-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,7,5 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 124754-67:
(8*1)+(7*2)+(6*4)+(5*7)+(4*5)+(3*4)+(2*6)+(1*7)=132
132 % 10 = 2
So 124754-67-2 is a valid CAS Registry Number.

124754-67-2Upstream product

124754-61-6 C₁₅H₃₀ClNO₂Si

124754-67-2Downstream Products

124754-67-2Relevant academic research and scientific papers

Syntheses and reactions of silyl carbamates. 2. A new mode of cyclic carbamate formation from tert-butyldimethylsilyl carbamate

Sakaitani, Masahiro,Ohfune, Yasufumi

, p. 1150 - 1158 (2007/10/02)

Stereoselective construction of 1,2 and 1,3 amino hydroxyl systems was achieved by the intramolecular trapping of the N-tert-butyldimethylsilyloxycarbonyl species (silyl carbamate) activated by fluoride ion. The reaction of the silyl carbamate with 1,2-sy

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