Cas 1388663-91-9,(R)-tert-butyl 2,2-dimethyl-4-(1-tosyl-1H-indol-3-yl)oxazolidine-3-carboxylate

1388663-91-9

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Basic information

Product Name: (R)-tert-butyl 2,2-dimethyl-4-(1-tosyl-1H-indol-3-yl)oxazolidine-3-carboxylate
Synonyms: (R)-tert-butyl 2,2-dimethyl-4-(1-tosyl-1H-indol-3-yl)oxazolidine-3-carboxylate
CAS NO:1388663-91-9
Molecular Formula:
Molecular Weight: 470.59
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 2,2-dimethyl-4-(1-tosyl-1H-indol-3-yl)oxazolidine-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (R)-tert-butyl 2,2-dimethyl-4-(1-tosyl-1H-indol-3-yl)oxazolidine-3-carboxylate(1388663-91-9)
EPA Substance Registry System: (R)-tert-butyl 2,2-dimethyl-4-(1-tosyl-1H-indol-3-yl)oxazolidine-3-carboxylate(1388663-91-9)

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: 1388663-91-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1388663-91-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,8,6,6 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1388663-91:
(9*1)+(8*3)+(7*8)+(6*8)+(5*6)+(4*6)+(3*3)+(2*9)+(1*1)=219
219 % 10 = 9
So 1388663-91-9 is a valid CAS Registry Number.

1388663-91-9Upstream product

1388663-87-3 (R)-tert-butyl 2,2-dimethyl-4-(2-(trimethylsilyl)-1-tosyl-1H-indol-3-yl)oxazolidine-3-carboxylate

1388663-91-9Downstream Products

1388663-91-9Relevant academic research and scientific papers

Synthesis of optically active 2- and 3- indolylglycine derivatives and their oxygen analogues

Goswami, Koushik,Duttagupta, Indranil,Sinha, Surajit

, p. 7081 - 7085 (2012)

2-Indolylglycine derivative and its oxygen analogue have been synthesized by Sonogashira coupling followed by cyclization in one pot between 2-iodoheteroarenes and ethynyloxazolidinone where 3-indolylglycine derivative and its oxygen analogue have been sy

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