Cas 1449604-87-8,tert-butyl (R)-3-[(S)-2-(diethoxyphosphoryl)-3-ethoxy-3-oxopropyl]-5-methyl-2-oxo-3-phenylindoline-1-carboxylate

1449604-87-8

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Basic information

Product Name: tert-butyl (R)-3-[(S)-2-(diethoxyphosphoryl)-3-ethoxy-3-oxopropyl]-5-methyl-2-oxo-3-phenylindoline-1-carboxylate
Synonyms:
CAS NO:1449604-87-8
Molecular Formula:
Molecular Weight: 559.596
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 (R)-3-[(S)-2-(diethoxyphosphoryl)-3-ethoxy-3-oxopropyl]-5-methyl-2-oxo-3-phenylindoline-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (R)-3-[(S)-2-(diethoxyphosphoryl)-3-ethoxy-3-oxopropyl]-5-methyl-2-oxo-3-phenylindoline-1-carboxylate(1449604-87-8)
EPA Substance Registry System: tert-butyl (R)-3-[(S)-2-(diethoxyphosphoryl)-3-ethoxy-3-oxopropyl]-5-methyl-2-oxo-3-phenylindoline-1-carboxylate(1449604-87-8)

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: 1449604-87-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1449604-87-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,9,6,0 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1449604-87:
(9*1)+(8*4)+(7*4)+(6*9)+(5*6)+(4*0)+(3*4)+(2*8)+(1*7)=188
188 % 10 = 8
So 1449604-87-8 is a valid CAS Registry Number.

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1449604-87-8Relevant academic research and scientific papers

Chiral squaramide catalyzed asymmetric conjugate additions of 3-substituted oxindoles to vinylphosphonates

Duan, Shu-Wen,Liu, Yi-Yin,Ding, Wei,Li, Tian-Ren,Shi, De-Qing,Chen, Jia-Rong,Xiao, Wen-Jing

, p. 1647 - 1653 (2013/07/27)

An efficient organocatalytic enantioselective conjugate addition of 3-substituted oxindoles to activated vinylphosphonates has been described. This reaction allows the facile synthesis of a new family of organophosphorus derivatives bearing an oxindole motif in high chemical yields with good to excellent stereoselectivities. Georg Thieme Verlag Stuttgart, New York.

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