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Carbamic acid, [(1S)-2-hydroxy-1-methyl-2-phenylethyl]-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

225098-33-9

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225098-33-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 225098-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,5,0,9 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 225098-33:
(8*2)+(7*2)+(6*5)+(5*0)+(4*9)+(3*8)+(2*3)+(1*3)=129
129 % 10 = 9
So 225098-33-9 is a valid CAS Registry Number.

225098-33-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-utyl ((2S)-1-hydroxy-1-phenylpropan-2-yl)carbamate

1.2 Other means of identification

Product number -
Other names (1RS,2S)-N-(tert-butyloxycarbonyl)norephedrine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:225098-33-9 SDS

225098-33-9Relevant academic research and scientific papers

A Simple Method for Chelation Controlled Additions to α-Amino Aldehydes

Reetz, Manfred T.,Roelfing, Karin,Griebenow, Nils

, p. 1969 - 1972 (1994)

BOC- and Cbz-protected α-amino aldehydes derived from amino acids undergo stereoselective addition reactions with alkyl cuprates and manganese reagents, the chelation-controlled adducts being the major diastereomers (generally ds > 90percent).Undesired ra

A novel linking-protecting group strategy for solid-phase organic chemistry with configurationally stable α-[N-(phenylfluorenyl)]amino carbonyl compounds: Synthesis of enantiopure norephedrines on solid support

Gosselin,Van Betsbrugge,Hatam,Lubell

, p. 2486 - 2493 (2007/10/03)

A novel linking strategy has been developed for synthesizing configurationally stable α-amino aldehyde on polymeric supports. Alkylation of L-alanine methyl ester with 9-bromo-9-p-bromophenylfluorenene, followed by ester hydrolysis and coupling to isoxazolidine, provided N-(9-p- bromophenylfluoren-9-yl)alanine isoxazolidide (5), which was transformed into its corresponding boronate 2 by a palladium-catalyzed cross-coupling reaction with diboron pinacol ester. Boronate 2 was anchored to four different polymeric aryl halides 6-9 in 70-99% yields. Polymer-bound alaninal 1b was then synthesized on non-cross-linked polystyrene by hydride reduction of isoxazolidide 10b. Treatment of alaninal 1b with phenylmagnesium bromide, cleavage of the resulting amino alcohol in a 1:2:2 TFA/CH2Cl2/anisole cocktail, and acylation with di-tert-butyl dicarbonate furnished N- (BOC)norephedrines 14 that were demonstrated to be enantiopure by conversion to diastereomeric thioureas 15 and analysis by HPLC. In summary, we have developed a process by which the 9-phenylfluoren-9-yl protecting group has been converted into a new linker for the solid-phase synthesis and manipulation of α-amino carbonyl compounds.

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