Cas 1174386-94-7,tert-butyl (2R,3R)-2-[(benzyloxy)methyl]-3-[(tert-butyldimethylsilyl)oxy]piperidine-1-carboxylate

1174386-94-7

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Basic information

Product Name: tert-butyl (2R,3R)-2-[(benzyloxy)methyl]-3-[(tert-butyldimethylsilyl)oxy]piperidine-1-carboxylate
Synonyms: tert-butyl (2R,3R)-2-[(benzyloxy)methyl]-3-[(tert-butyldimethylsilyl)oxy]piperidine-1-carboxylate
CAS NO:1174386-94-7
Molecular Formula:
Molecular Weight: 435.679
EINECS: N/A
Product Categories: N/A
Mol File: 1174386-94-7.mol
Article Data: 2

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 (2R,3R)-2-[(benzyloxy)methyl]-3-[(tert-butyldimethylsilyl)oxy]piperidine-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (2R,3R)-2-[(benzyloxy)methyl]-3-[(tert-butyldimethylsilyl)oxy]piperidine-1-carboxylate(1174386-94-7)
EPA Substance Registry System: tert-butyl (2R,3R)-2-[(benzyloxy)methyl]-3-[(tert-butyldimethylsilyl)oxy]piperidine-1-carboxylate(1174386-94-7)

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: 1174386-94-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1174386-94-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,4,3,8 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1174386-94:
(9*1)+(8*1)+(7*7)+(6*4)+(5*3)+(4*8)+(3*6)+(2*9)+(1*4)=177
177 % 10 = 7
So 1174386-94-7 is a valid CAS Registry Number.

1174386-94-7Upstream product

24424-99-5 di-tert-butyl dicarbonate

1174386-94-7Downstream Products

1174386-94-7Relevant articles and documents

Chiron approach to formal synthesis of both antipodes of cis 3-hydroxypipecolic acid

Chavan, Subhash P.,Khairnar, Lalit B.,Chavan, Prakash N.,Dumare, Nilesh B.,Kalbhor, Dinesh B.,Gonnade, Rajesh G.

, p. 6423 - 6426 (2014)

The efficient and practical formal syntheses of both enantiomers of cis 3-hydroxypipecolic acid were accomplished from cis aziridine-2-carboxylate as the common synthetic precursor. The key steps involved are stereo and regioselective aziridine ring openi

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