Cas 201655-58-5,(2R,4S)-3-(2-tert-Butoxycarbonyl-acetyl)-2-tert-butyl-oxazolidine-4-carboxylic acid methyl ester

201655-58-5

Post Buying Request

Basic information

Product Name: (2R,4S)-3-(2-tert-Butoxycarbonyl-acetyl)-2-tert-butyl-oxazolidine-4-carboxylic acid methyl ester
Synonyms: (2R,4S)-3-(2-tert-Butoxycarbonyl-acetyl)-2-tert-butyl-oxazolidine-4-carboxylic acid methyl ester
CAS NO:201655-58-5
Molecular Formula:
Molecular Weight: 329.393
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,4S)-3-(2-tert-Butoxycarbonyl-acetyl)-2-tert-butyl-oxazolidine-4-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2R,4S)-3-(2-tert-Butoxycarbonyl-acetyl)-2-tert-butyl-oxazolidine-4-carboxylic acid methyl ester(201655-58-5)
EPA Substance Registry System: (2R,4S)-3-(2-tert-Butoxycarbonyl-acetyl)-2-tert-butyl-oxazolidine-4-carboxylic acid methyl ester(201655-58-5)

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: 201655-58-5(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

201655-58-5 Suppliers

Recommended suppliers

201655-58-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 201655-58-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,6,5 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 201655-58:
(8*2)+(7*0)+(6*1)+(5*6)+(4*5)+(3*5)+(2*5)+(1*8)=105
105 % 10 = 5
So 201655-58-5 is a valid CAS Registry Number.

201655-58-5Upstream product

201655-58-5Downstream Products

201655-58-5Relevant academic research and scientific papers

Regioselective Dieckmann cyclisations leading to enantiopure highly functionalised tetramic acid derivatives

Andrews, Mark D.,Brewster, Andrew G.,Crapnell, Katherine M.,Ibbett, Ashley J.,Jones, Tim,Moloney, Mark G.,Prout, Keith,Watkin, David

, p. 223 - 235 (2007/10/03)

Regioselective Dieckmann cyclisations using an N-acyloxazolidine derived from L-serine give substituted tetramic acids in high yield and enantioselectivity. The products are easily deprotected under mild conditions to give hydroxymethyltetramic acids.

Post a RFQ

Cas No.:

Product Name:

Quantity:

Email:

Company name:

Valid Period:

Detailed Requirements:

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

What can I do for you?
Get Best Price

Get Best Price for 201655-58-5