Cas 1374450-33-5,(R)-tert-butyl 1-((S)-(benzyloxycarbonylamino)(m-tolyl)methyl)-6-bromo-3-oxo-1,3-dihydroisobenzofuran-1-carboxylate

1374450-33-5

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Basic information

Product Name: (R)-tert-butyl 1-((S)-(benzyloxycarbonylamino)(m-tolyl)methyl)-6-bromo-3-oxo-1,3-dihydroisobenzofuran-1-carboxylate
Synonyms:
CAS NO:1374450-33-5
Molecular Formula:
Molecular Weight: 566.448
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: (R)-tert-butyl 1-((S)-(benzyloxycarbonylamino)(m-tolyl)methyl)-6-bromo-3-oxo-1,3-dihydroisobenzofuran-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (R)-tert-butyl 1-((S)-(benzyloxycarbonylamino)(m-tolyl)methyl)-6-bromo-3-oxo-1,3-dihydroisobenzofuran-1-carboxylate(1374450-33-5)
EPA Substance Registry System: (R)-tert-butyl 1-((S)-(benzyloxycarbonylamino)(m-tolyl)methyl)-6-bromo-3-oxo-1,3-dihydroisobenzofuran-1-carboxylate(1374450-33-5)

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: 1374450-33-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1374450-33-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,4,5 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1374450-33:
(9*1)+(8*3)+(7*7)+(6*4)+(5*4)+(4*5)+(3*0)+(2*3)+(1*3)=155
155 % 10 = 5
So 1374450-33-5 is a valid CAS Registry Number.

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1374450-33-5Relevant academic research and scientific papers

Direct asymmetric Mannich reaction of phthalides: Facile access to chiral substituted isoquinolines and isoquinolinones

Luo, Jie,Wang, Haifei,Zhong, Fangrui,Kwiatkowski, Jacek,Xu, Li-Wen,Lu, Yixin

, p. 4707 - 4709 (2012/06/29)

The first Mannich reaction employing phthalides using a quinidine-based multifunctional catalyst has been developed. The reported method led to the synthesis of 3,3-disubstituted phthalide derivatives in excellent yields, with good diastereo- and enantioselectivities. Convenient synthesis of chiral isoquinolinones and isoquinolines has also been demonstrated.

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