Cas 1403986-71-9,4-(4-i-propylphenyl)-1,5-dioxo-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinazoline-3a-carboxylic acid

1403986-71-9

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Basic information

Product Name: 4-(4-i-propylphenyl)-1,5-dioxo-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinazoline-3a-carboxylic acid
Synonyms: 4-(4-i-propylphenyl)-1,5-dioxo-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinazoline-3a-carboxylic acid
CAS NO:1403986-71-9
Molecular Formula:
Molecular Weight: 364.401
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: 4-(4-i-propylphenyl)-1,5-dioxo-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinazoline-3a-carboxylic acid(CAS DataBase Reference)
NIST Chemistry Reference: 4-(4-i-propylphenyl)-1,5-dioxo-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinazoline-3a-carboxylic acid(1403986-71-9)
EPA Substance Registry System: 4-(4-i-propylphenyl)-1,5-dioxo-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinazoline-3a-carboxylic acid(1403986-71-9)

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: 1403986-71-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1403986-71-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,9,8 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1403986-71:
(9*1)+(8*4)+(7*0)+(6*3)+(5*9)+(4*8)+(3*6)+(2*7)+(1*1)=169
169 % 10 = 9
So 1403986-71-9 is a valid CAS Registry Number.

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1403986-71-9Relevant academic research and scientific papers

Iodine-catalyzed synthesis of pyrrolo[1,2-a]quinazoline-3a-carboxylic acid derivatives in ionic liquids

Zhang, Mei-Mei,Lu, Lian,Zhou, Yu-Jing,Wang, Xiang-Shan

, p. 3327 - 3335 (2013/09/23)

The iodine-catalyzed reaction of 2-aminobenzamide and 2-oxopentanedioic acid in ionic liquids is described in this paper. It gave 1,5-dioxo-1,2,3,3a,4, 5-hexahydropyrrolo[1,2-a]quinazoline-3a-carboxylic acid derivatives in high yields. One of their struct

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