Cas 134932-45-9,N-methyl 2(R),6(R),7(R),8(S) 2-phenyl-1-aza-4-oxa<4.3.0<sup>1,6</sup>>bicyclononan-5-one-7,8-dicarboximide

134932-45-9

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Basic information

Product Name: N-methyl 2(R),6(R),7(R),8(S) 2-phenyl-1-aza-4-oxa<4.3.0^1,6>bicyclononan-5-one-7,8-dicarboximide
Synonyms:
CAS NO:134932-45-9
Molecular Formula:
Molecular Weight: 300.314
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: N-methyl 2(R),6(R),7(R),8(S) 2-phenyl-1-aza-4-oxa<4.3.0^1,6>bicyclononan-5-one-7,8-dicarboximide(CAS DataBase Reference)
NIST Chemistry Reference: N-methyl 2(R),6(R),7(R),8(S) 2-phenyl-1-aza-4-oxa<4.3.0^1,6>bicyclononan-5-one-7,8-dicarboximide(134932-45-9)
EPA Substance Registry System: N-methyl 2(R),6(R),7(R),8(S) 2-phenyl-1-aza-4-oxa<4.3.0^1,6>bicyclononan-5-one-7,8-dicarboximide(134932-45-9)

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: 134932-45-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 134932-45-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,9,3 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 134932-45:
(8*1)+(7*3)+(6*4)+(5*9)+(4*3)+(3*2)+(2*4)+(1*5)=129
129 % 10 = 9
So 134932-45-9 is a valid CAS Registry Number.

134932-45-9Upstream product

134932-45-9Downstream Products

134932-45-9Relevant academic research and scientific papers

Development of chiral stabilised azomethine ylids: A chiral memory relay system

Anslow,Harwood,Phillips,Watkin,Wong

, p. 1343 - 1358 (2007/10/02)

Chiral, stabilised azomethine ylids incorporated in cyclic templates derived from (R)- or (S)-2-phenylglycinol and (S)-valine undergo enantioselective 1,3-dipolar cycloaddition reactions with a variety of dipolarophiles. Removal of the template in the cas

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