Cas 1532520-65-2,tert-butyl 2,3-dimethoxy-9,11-dioxo-10-phenyl-6,9,10,11-tetrahydro-5H-pyrrolo[3′,4′:3,4]pyrrolo[2,1-a]isoquinoline-8-carboxylate

1532520-65-2

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Basic information

Product Name: tert-butyl 2,3-dimethoxy-9,11-dioxo-10-phenyl-6,9,10,11-tetrahydro-5H-pyrrolo[3′,4′:3,4]pyrrolo[2,1-a]isoquinoline-8-carboxylate
Synonyms: tert-butyl 2,3-dimethoxy-9,11-dioxo-10-phenyl-6,9,10,11-tetrahydro-5H-pyrrolo[3′,4′:3,4]pyrrolo[2,1-a]isoquinoline-8-carboxylate
CAS NO:1532520-65-2
Molecular Formula:
Molecular Weight: 414.461
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: tert-butyl 2,3-dimethoxy-9,11-dioxo-10-phenyl-6,9,10,11-tetrahydro-5H-pyrrolo[3′,4′:3,4]pyrrolo[2,1-a]isoquinoline-8-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl 2,3-dimethoxy-9,11-dioxo-10-phenyl-6,9,10,11-tetrahydro-5H-pyrrolo[3′,4′:3,4]pyrrolo[2,1-a]isoquinoline-8-carboxylate(1532520-65-2)
EPA Substance Registry System: tert-butyl 2,3-dimethoxy-9,11-dioxo-10-phenyl-6,9,10,11-tetrahydro-5H-pyrrolo[3′,4′:3,4]pyrrolo[2,1-a]isoquinoline-8-carboxylate(1532520-65-2)

Safety Data

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Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1532520-65-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1532520-65-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,3,2,5,2 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1532520-65:
(9*1)+(8*5)+(7*3)+(6*2)+(5*5)+(4*2)+(3*0)+(2*6)+(1*5)=132
132 % 10 = 2
So 1532520-65-2 is a valid CAS Registry Number.

1532520-65-2Upstream product

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1532520-65-2Relevant academic research and scientific papers

A general, simple and green process to access pyrrolo[2,1-a]isoquinolines using a KI/TBHP catalytic system

Huang, Huan-Ming,Huang, Fang,Li, Yu-Jin,Jia, Jian-Hong,Ye, Qing,Han, Liang,Gao, Jian-Rong

, p. 27250 - 27258 (2014)

A novel KI/TBHP-catalyzed 1,3-dipolar cycloaddition/oxidation/aromatization cascade reaction provided general, efficient and green access to biologically important pyrrolo[2,1-a]isoquinolines. The product pyrrolo[2,1-a]isoquinolines were obtained from rea

CuBr/NHPI co-catalyzed aerobic oxidative [3 + 2] cycloaddition-aromatization to access 5,6-dihydro-pyrrolo[2,1-: A] isoquinolines

Xie, Zhiyu,Li, Fei,Niu, Liangfeng,Li, Hongbing,Zheng, Jincai,Han, Ruijing,Ju, Zhiyu,Li, Shanshan,Li, Dandan

, p. 6889 - 6898 (2020/10/02)

An efficient and enviromentally friendly CuBr/NHPI co-catalyzed aerobic oxidative [3 + 2] cycloaddition-aromatization cascade was realized with N-substituted tetrahydroisoquinolines and electron-deficient olefins. Under the mild conditions, the reaction p

Pyrrole [2,1-a] isoquinoline alkaloid and preparation method and application thereof

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Paragraph 0057; 0091; 0092; 0093, (2018/03/24)

The invention discloses pyrrole [2,1-a] isoquinoline alkaloid and a preparation method and medical application thereof, and belongs to the field of medicinal chemistry. The structural general formula of the pyrrole [2,1-a] isoquinoline alkaloid is as show

TBAI/TBHP-catalyzed [3 + 2]cycloaddition/oxidation/aromatization cascade and online ESI-MS mechanistic studies: Synthesis of pyrrolo[2,1-a]isoquinolines and indolizino[8,7-b]indoles

Nekkanti, Shalini,Kumar, Niggula Praveen,Sharma, Pankaj,Kamal, Ahmed,Nachtigall, Fabiane M.,Forero-Doria, Oscar,Santos, Leonardo S.,Shankaraiah, Nagula

, p. 2671 - 2677 (2016/01/16)

A facile [3 + 2]cycloaddition/oxidation/aromatization cascade reaction for the synthesis of pyrrolo[2,1-a]isoquinolines and indolizino[8,7-b]indoles has been developed. This tandem approach was accomplished by employing tert-butyl hydroperoxide (TBHP) as

Iodine-catalyzed 1,3-dipolar cycloaddition/oxidation/aromatization cascade with hydrogen peroxide as the terminal oxidant: General route to pyrrolo[2,1- a ]isoquinolines

Huang, Huan-Ming,Li, Yu-Jin,Ye, Qing,Yu, Wu-Bin,Han, Liang,Jia, Jian-Hong,Gao, Jian-Rong

, p. 1084 - 1092 (2014/03/21)

We report a novel molecular iodine-catalyzed 1,3-dipolar cycloaddition/oxidation/aromatization cascade process with hydrogen peroxide as the terminal oxidant for the construction of pyrrolo[2,1-a]isoquinolines. The product pyrrolo[2,1-a]isoquinolines were

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