Cas 1052273-41-2,(2R,3S)-2-tert-butoxycarbonylamino-5-(2,6-dimethyl-4-nitro-phenoxy)-3-hydroxy-pentanoic acid methyl ester

1052273-41-2

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Basic information

Product Name: (2R,3S)-2-tert-butoxycarbonylamino-5-(2,6-dimethyl-4-nitro-phenoxy)-3-hydroxy-pentanoic acid methyl ester
Synonyms: (2R,3S)-2-tert-butoxycarbonylamino-5-(2,6-dimethyl-4-nitro-phenoxy)-3-hydroxy-pentanoic acid methyl ester
CAS NO:1052273-41-2
Molecular Formula:
Molecular Weight: 412.44
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: (2R,3S)-2-tert-butoxycarbonylamino-5-(2,6-dimethyl-4-nitro-phenoxy)-3-hydroxy-pentanoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S)-2-tert-butoxycarbonylamino-5-(2,6-dimethyl-4-nitro-phenoxy)-3-hydroxy-pentanoic acid methyl ester(1052273-41-2)
EPA Substance Registry System: (2R,3S)-2-tert-butoxycarbonylamino-5-(2,6-dimethyl-4-nitro-phenoxy)-3-hydroxy-pentanoic acid methyl ester(1052273-41-2)

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: 1052273-41-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1052273-41-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,2,2,7 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1052273-41:
(9*1)+(8*0)+(7*5)+(6*2)+(5*2)+(4*7)+(3*3)+(2*4)+(1*1)=112
112 % 10 = 2
So 1052273-41-2 is a valid CAS Registry Number.

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1052273-41-2Relevant academic research and scientific papers

The Sharpless asymmetric aminohydroxylation reaction: Optimising ligand/substrate control of regioselectivity for the synthesis of 3- and 4-aminosugars

Bodkin, Jennifer A.,Bacskay, George B.,McLeod, Malcolm D.

experimental part, p. 2544 - 2553 (2009/02/02)

An investigation of the factors responsible for the sense and magnitude of regioselectivity in the Sharpless asymmetric aminohydroxylation (AA) has been conducted. Theoretical investigations of ligand-osmium binding geometry and experimental investigation

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