Cas 1260161-70-3,3-tert-butyl-7-(4-chlorobenzyl)-1-phenyl-1,4,6,7-tetrahydropyrazolo-[3,4-d][1,3]oxazine

1260161-70-3

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Basic information

Product Name: 3-tert-butyl-7-(4-chlorobenzyl)-1-phenyl-1,4,6,7-tetrahydropyrazolo-[3,4-d][1,3]oxazine
Synonyms: 3-tert-butyl-7-(4-chlorobenzyl)-1-phenyl-1,4,6,7-tetrahydropyrazolo-[3,4-d][1,3]oxazine
CAS NO:1260161-70-3
Molecular Formula:
Molecular Weight: 381.905
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: 3-tert-butyl-7-(4-chlorobenzyl)-1-phenyl-1,4,6,7-tetrahydropyrazolo-[3,4-d][1,3]oxazine(CAS DataBase Reference)
NIST Chemistry Reference: 3-tert-butyl-7-(4-chlorobenzyl)-1-phenyl-1,4,6,7-tetrahydropyrazolo-[3,4-d][1,3]oxazine(1260161-70-3)
EPA Substance Registry System: 3-tert-butyl-7-(4-chlorobenzyl)-1-phenyl-1,4,6,7-tetrahydropyrazolo-[3,4-d][1,3]oxazine(1260161-70-3)

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: 1260161-70-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1260161-70-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,1,6 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1260161-70:
(9*1)+(8*2)+(7*6)+(6*0)+(5*1)+(4*6)+(3*1)+(2*7)+(1*0)=113
113 % 10 = 3
So 1260161-70-3 is a valid CAS Registry Number.

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1260161-70-3Relevant academic research and scientific papers

An Efficient Synthesis of 7-(Arylmethyl)-3-tert-butyl-1-phenyl-6,7-dihydro- 1H,4H-pyrazolo[3,4-d][1,3]oxazines

Abonia, Rodrigo,Castillo, Juan,Insuasty, Braulio,Quiroga, Jairo,Nogueras, Manuel,Cobo, Justo

experimental part, p. 6454 - 6463 (2011/02/21)

An efficient and three-step procedure for the synthesis of novel 6,7-dihydro-1H,4H-pyrazolo[3,4-d][1,3]oxazine derivatives in good to excellent yields by treatment of pyrazolamines with aqueous formaldehyde in the presence of acetic acid is provided. The

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