Cas 219671-17-7,methyl 4-(benzyloxy)-3-(N-tert-butoxycarbonylamino)butanoate

219671-17-7

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Basic information

Product Name: methyl 4-(benzyloxy)-3-(N-tert-butoxycarbonylamino)butanoate
Synonyms: methyl 4-(benzyloxy)-3-(N-tert-butoxycarbonylamino)butanoate
CAS NO:219671-17-7
Molecular Formula:
Molecular Weight: 323.389
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: methyl 4-(benzyloxy)-3-(N-tert-butoxycarbonylamino)butanoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 4-(benzyloxy)-3-(N-tert-butoxycarbonylamino)butanoate(219671-17-7)
EPA Substance Registry System: methyl 4-(benzyloxy)-3-(N-tert-butoxycarbonylamino)butanoate(219671-17-7)

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: 219671-17-7(Hazardous Substances Data)

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219671-17-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 219671-17-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,6,7 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 219671-17:
(8*2)+(7*1)+(6*9)+(5*6)+(4*7)+(3*1)+(2*1)+(1*7)=147
147 % 10 = 7
So 219671-17-7 is a valid CAS Registry Number.

219671-17-7Upstream product

77086-38-5 ketene t-butyldimethylsilyl methyl acetal

219671-17-7Downstream Products

219671-17-7Relevant academic research and scientific papers

Catalyst-free Mannich-type reaction of 1-(N-acylamino)alkyltriphenylphosphonium salts with silyl enolates

Pa?dzierniok-Holewa, Agnieszka,Wal?cka-Kurczyk, Alicja,Musio?, Szymon,Stecko, Sebastian

, p. 732 - 742 (2019)

A catalyst-free reaction of 1-(N-acylamino)alkyltriphenylphosphonium tetrafluoroborates with silyl enolates was developed to prepare β-amino carbonyl compounds. The reported method is a useful approach for the preparation of N-protected β-amino esters as

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