Cas 132576-03-5,2-Phenyl-1,8-dioxa-2-aza-spiro[4.5]decane-3-carboxylic acid phenylamide

132576-03-5

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Basic information

Product Name: 2-Phenyl-1,8-dioxa-2-aza-spiro[4.5]decane-3-carboxylic acid phenylamide
Synonyms: 2-Phenyl-1,8-dioxa-2-aza-spiro[4.5]decane-3-carboxylic acid phenylamide
CAS NO:132576-03-5
Molecular Formula:
Molecular Weight: 338.406
EINECS: N/A
Product Categories: N/A
Mol File: 132576-03-5.mol
Article Data: 1

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: 2-Phenyl-1,8-dioxa-2-aza-spiro[4.5]decane-3-carboxylic acid phenylamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-Phenyl-1,8-dioxa-2-aza-spiro[4.5]decane-3-carboxylic acid phenylamide(132576-03-5)
EPA Substance Registry System: 2-Phenyl-1,8-dioxa-2-aza-spiro[4.5]decane-3-carboxylic acid phenylamide(132576-03-5)

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: 132576-03-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 132576-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,7 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 132576-03:
(8*1)+(7*3)+(6*2)+(5*5)+(4*7)+(3*6)+(2*0)+(1*3)=115
115 % 10 = 5
So 132576-03-5 is a valid CAS Registry Number.

132576-03-5Upstream product

132576-03-5Downstream Products

132576-03-5Relevant articles and documents

REACTIONS OF NITRONES WITH DI- AND TETRAHYDROPYRANS

Sagitdinova, Kh. F.,Ibatullin, U. G.,Gallyamova, Z. R.,Rakhmatullina, G. A.,Akmanova, N. A.,Safarov, M. G.

, p. 932 - 935 (1990)

N-(Benzylidene)- and N-(2-phenylamino-2-oxoethylidene)aniline N-oxides add stereospecifically to the double bond in 4-methylene- and 4-acryloylamino-4-methyltetrahydropyrans to give substituted isoxazolidines.The use of 4-methyl-5-arylamino- and 4-arylami

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