Cas 872864-63-6,Carbamic acid, [(1R)-1-(hydroxymethyl)-3-(4-nitrophenoxy)propyl]-, 2-(trimethylsilyl)ethyl ester

872864-63-6

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Basic information

Product Name: Carbamic acid, [(1R)-1-(hydroxymethyl)-3-(4-nitrophenoxy)propyl]-, 2-(trimethylsilyl)ethyl ester
Synonyms:
CAS NO:872864-63-6
Molecular Formula: C16H26N2O6Si
Molecular Weight: 370.478
EINECS: N/A
Product Categories: N/A
Mol File: 872864-63-6.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: Carbamic acid, [(1R)-1-(hydroxymethyl)-3-(4-nitrophenoxy)propyl]-, 2-(trimethylsilyl)ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [(1R)-1-(hydroxymethyl)-3-(4-nitrophenoxy)propyl]-, 2-(trimethylsilyl)ethyl ester(872864-63-6)
EPA Substance Registry System: Carbamic acid, [(1R)-1-(hydroxymethyl)-3-(4-nitrophenoxy)propyl]-, 2-(trimethylsilyl)ethyl ester(872864-63-6)

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: 872864-63-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 872864-63-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,8,6 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 872864-63:
(8*8)+(7*7)+(6*2)+(5*8)+(4*6)+(3*4)+(2*6)+(1*3)=216
216 % 10 = 6
So 872864-63-6 is a valid CAS Registry Number.

872864-63-6Upstream product

872864-63-6Downstream Products

872864-63-6Relevant articles and documents

The asymmetric aminohydroxylation route to GABOB and homoserine derivatives

Harding, Michael,Bodkin, Jennifer A.,Issa, Fatiah,Hutton, Craig A.,Willis, Anthony C.,McLeod, Malcolm D.

experimental part, p. 831 - 843 (2009/04/07)

The 4-nitrophenyl ether is an efficient directing group in the asymmetric aminohydroxylation reaction of homoallylic ether derivatives. Either regioisomeric product can be obtained with useful levels of enantioselectivity allowing for the short enantiosel

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