Cas 1391858-22-2,(2'S,3'R,4'S)-5',5'-diethyl 3',4'-dimethyl 1-benzyl-6-methyl-2-oxospiro[indoline-3,2'-pyrrolidine]-3',4',5',5'-tetracarboxylate

1391858-22-2

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Basic information

Product Name: (2'S,3'R,4'S)-5',5'-diethyl 3',4'-dimethyl 1-benzyl-6-methyl-2-oxospiro[indoline-3,2'-pyrrolidine]-3',4',5',5'-tetracarboxylate
Synonyms: (2'S,3'R,4'S)-5',5'-diethyl 3',4'-dimethyl 1-benzyl-6-methyl-2-oxospiro[indoline-3,2'-pyrrolidine]-3',4',5',5'-tetracarboxylate
CAS NO:1391858-22-2
Molecular Formula:
Molecular Weight: 552.581
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: (2'S,3'R,4'S)-5',5'-diethyl 3',4'-dimethyl 1-benzyl-6-methyl-2-oxospiro[indoline-3,2'-pyrrolidine]-3',4',5',5'-tetracarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (2'S,3'R,4'S)-5',5'-diethyl 3',4'-dimethyl 1-benzyl-6-methyl-2-oxospiro[indoline-3,2'-pyrrolidine]-3',4',5',5'-tetracarboxylate(1391858-22-2)
EPA Substance Registry System: (2'S,3'R,4'S)-5',5'-diethyl 3',4'-dimethyl 1-benzyl-6-methyl-2-oxospiro[indoline-3,2'-pyrrolidine]-3',4',5',5'-tetracarboxylate(1391858-22-2)

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: 1391858-22-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1391858-22-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,1,8,5 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1391858-22:
(9*1)+(8*3)+(7*9)+(6*1)+(5*8)+(4*5)+(3*8)+(2*2)+(1*2)=192
192 % 10 = 2
So 1391858-22-2 is a valid CAS Registry Number.

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1391858-22-2Relevant academic research and scientific papers

Scaffold-inspired enantioselective synthesis of biologically important spiro[pyrrolidin-3,2'-oxindoles] with structural diversity through catalytic isatin-derived 1,3-dipolar cycloadditions

Shi, Feng,Tao, Zhong-Lin,Luo, Shi-Wei,Tu, Shu-Jiang,Gong, Liu-Zhu

supporting information; experimental part, p. 6885 - 6894 (2012/07/27)

Catalytic asymmetric construction of the biologically important spiro[pyrrolidin-3,2'-oxindole] scaffold with contiguous quaternary stereogenic centers in excellent stereoselectivities (up to >99:1 d.r., 98 % ee) has been established by using an organocat

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