Cas 1416352-40-3,(R)-tert-butyl 4-(1,3-dioxolan-2-yl)-2-(diphenylmethyleneamino)butanoate

1416352-40-3

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Basic information

Product Name: (R)-tert-butyl 4-(1,3-dioxolan-2-yl)-2-(diphenylmethyleneamino)butanoate
Synonyms: (R)-tert-butyl 4-(1,3-dioxolan-2-yl)-2-(diphenylmethyleneamino)butanoate
CAS NO:1416352-40-3
Molecular Formula:
Molecular Weight: 395.499
EINECS: N/A
Product Categories: N/A
Mol File: 1416352-40-3.mol
Article Data: 1

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 4-(1,3-dioxolan-2-yl)-2-(diphenylmethyleneamino)butanoate(CAS DataBase Reference)
NIST Chemistry Reference: (R)-tert-butyl 4-(1,3-dioxolan-2-yl)-2-(diphenylmethyleneamino)butanoate(1416352-40-3)
EPA Substance Registry System: (R)-tert-butyl 4-(1,3-dioxolan-2-yl)-2-(diphenylmethyleneamino)butanoate(1416352-40-3)

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: 1416352-40-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1416352-40-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,6,3,5 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1416352-40:
(9*1)+(8*4)+(7*1)+(6*6)+(5*3)+(4*5)+(3*2)+(2*4)+(1*0)=133
133 % 10 = 3
So 1416352-40-3 is a valid CAS Registry Number.

1416352-40-3Upstream product

1416352-40-3Downstream Products

2812-46-6 L-proline t-butyl ester

1416352-40-3Relevant articles and documents

Stereoselective synthesis of cyclic amino acids via asymmetric phase-transfer catalytic alkylation

Kano, Taichi,Kumano, Takeshi,Sakamoto, Ryu,Maruoka, Keiji

supporting information, p. 271 - 278 (2013/02/25)

An asymmetric synthesis of cyclic amino acids having piperidine and azepane core structures was realized starting from readily available glycine and alanine esters by combination of phase-transfer catalyzed asymmetric alkylation and subsequent reductive a

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