Cas 1375007-98-9,[(N,N,N',N'-tetramethylethylenediamine)Na(2,2,6,6-tetramethylpiperidide)(α-C4H7NBoc)Zn(tBu)]

1375007-98-9

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Basic information

Product Name: [(N,N,N',N'-tetramethylethylenediamine)Na(2,2,6,6-tetramethylpiperidide)(α-C4H7NBoc)Zn(tBu)]
Synonyms: [(N,N,N',N'-tetramethylethylenediamine)Na(2,2,6,6-tetramethylpiperidide)(α-C4H7NBoc)Zn(tBu)]
CAS NO:1375007-98-9
Molecular Formula:
Molecular Weight: 572.182
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: [(N,N,N',N'-tetramethylethylenediamine)Na(2,2,6,6-tetramethylpiperidide)(α-C4H7NBoc)Zn(tBu)](CAS DataBase Reference)
NIST Chemistry Reference: [(N,N,N',N'-tetramethylethylenediamine)Na(2,2,6,6-tetramethylpiperidide)(α-C4H7NBoc)Zn(tBu)](1375007-98-9)
EPA Substance Registry System: [(N,N,N',N'-tetramethylethylenediamine)Na(2,2,6,6-tetramethylpiperidide)(α-C4H7NBoc)Zn(tBu)](1375007-98-9)

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: 1375007-98-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1375007-98-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,5,0,0 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1375007-98:
(9*1)+(8*3)+(7*7)+(6*5)+(5*0)+(4*0)+(3*7)+(2*9)+(1*8)=159
159 % 10 = 9
So 1375007-98-9 is a valid CAS Registry Number.

1375007-98-9Upstream product

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1375007-98-9Relevant academic research and scientific papers

Ambient temperature zincation of N-Boc pyrrolidine and its solvent dependency

Garden, Jennifer A.,Kennedy, Alan R.,Mulvey, Robert E.,Robertson, Stuart D.

, p. 5265 - 5267 (2012)

Sodium TMP-zincate, [(TMEDA)Na(TMP)(tBu)Zn(tBu)], can deproto-zincate N-Boc pyrrolidine at ambient temperature in hexane solution, whereas in toluene the captured α-carbanion of the heterocycle attacks the solvent setting off a cascade of reactions that ultimately produce a pyrrolidine-substituted enolate.

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