Cas 1377322-22-9,(3R,4S)-benzyl 9-acetyl-3-(3-(benzyloxy)propyl)-2-oxo-2,3,4,9-tetrahydropyrano[2,3-b]indole-4-carboxylate

1377322-22-9

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Basic information

Product Name: (3R,4S)-benzyl 9-acetyl-3-(3-(benzyloxy)propyl)-2-oxo-2,3,4,9-tetrahydropyrano[2,3-b]indole-4-carboxylate
Synonyms: (3R,4S)-benzyl 9-acetyl-3-(3-(benzyloxy)propyl)-2-oxo-2,3,4,9-tetrahydropyrano[2,3-b]indole-4-carboxylate
CAS NO:1377322-22-9
Molecular Formula:
Molecular Weight: 511.574
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: (3R,4S)-benzyl 9-acetyl-3-(3-(benzyloxy)propyl)-2-oxo-2,3,4,9-tetrahydropyrano[2,3-b]indole-4-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4S)-benzyl 9-acetyl-3-(3-(benzyloxy)propyl)-2-oxo-2,3,4,9-tetrahydropyrano[2,3-b]indole-4-carboxylate(1377322-22-9)
EPA Substance Registry System: (3R,4S)-benzyl 9-acetyl-3-(3-(benzyloxy)propyl)-2-oxo-2,3,4,9-tetrahydropyrano[2,3-b]indole-4-carboxylate(1377322-22-9)

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: 1377322-22-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1377322-22-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,7,3,2 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1377322-22:
(9*1)+(8*3)+(7*7)+(6*7)+(5*3)+(4*2)+(3*2)+(2*2)+(1*2)=159
159 % 10 = 9
So 1377322-22-9 is a valid CAS Registry Number.

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1377322-22-9Relevant academic research and scientific papers

N -heterocyclic carbene (NHC)-catalyzed highly diastereo- and enantioselective oxo-Diels-Alder reactions for synthesis of fused pyrano[2,3- b ]indoles

Yang, Limin,Wang, Fei,Chua, Pei Juan,Lv, Yunbo,Zhong, Liang-Jun,Zhong, Guofu

, p. 2894 - 2897 (2012)

A chiral N-heterocyclic carbene (NHC)-catalyzed Diels-Alder reaction of 2-oxoindolin-3-ylidenes and α-chloroaldehydes was developed for the synthesis of fused pyrano[2,3-b]indoles in good to excellent yields (up to 99%) with high cis-diastereoselectivities (>99:1 dr) and enantioselectivities (up to >99% ee).

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