Cas 182874-93-7,4-(4-tert-Butoxycarbonyl-2,5-difluoro-phenoxy)-piperidine-1-carboxylic acid tert-butyl ester

182874-93-7

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Basic information

Product Name: 4-(4-tert-Butoxycarbonyl-2,5-difluoro-phenoxy)-piperidine-1-carboxylic acid tert-butyl ester
Synonyms: 4-(4-tert-Butoxycarbonyl-2,5-difluoro-phenoxy)-piperidine-1-carboxylic acid tert-butyl ester
CAS NO:182874-93-7
Molecular Formula:
Molecular Weight: 413.462
EINECS: N/A
Product Categories: N/A
Mol File: 182874-93-7.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: 4-(4-tert-Butoxycarbonyl-2,5-difluoro-phenoxy)-piperidine-1-carboxylic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-(4-tert-Butoxycarbonyl-2,5-difluoro-phenoxy)-piperidine-1-carboxylic acid tert-butyl ester(182874-93-7)
EPA Substance Registry System: 4-(4-tert-Butoxycarbonyl-2,5-difluoro-phenoxy)-piperidine-1-carboxylic acid tert-butyl ester(182874-93-7)

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: 182874-93-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 182874-93-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,8,7 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 182874-93:
(8*1)+(7*8)+(6*2)+(5*8)+(4*7)+(3*4)+(2*9)+(1*3)=177
177 % 10 = 7
So 182874-93-7 is a valid CAS Registry Number.

182874-93-7Upstream product

182874-93-7Downstream Products

182874-93-7Relevant articles and documents

Regioselective nucleophilic substitutions of fluorobenzene derivatives

Wells, Kenneth M.,Shi, Yao-Jun,Lynch, Joseph E.,Humphrey, Guy R.,Volante,Reider, Paul J.

, p. 6439 - 6442 (2007/10/03)

Regioselective nucleophilic substitutions of tri- and di-substituted fluorobenzoates, fluorobenzonitriles, and fluoronitrobenzenes were accomplished by sequential addition of various nucleophiles, such as, potassium N-Boc-4-piperidinyl oxide, potassium methoxide, and piperidine.

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