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115378-31-9

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115378-31-9 Usage

General Description

(R)-N-BOC-2,2-DIMETHYL-4-VINYLOXAZOLIDINE is a chemical compound that belongs to the oxazolidine family. It is a chiral compound, meaning it has a specific three-dimensional arrangement of atoms. The "R" in its name indicates the configuration of the compound's chiral center. (R)-N-BOC-2,2-DIMETHYL-4-VINYLOXAZOLIDINE is commonly used as a reagent in chemical synthesis, particularly in the production of pharmaceuticals and other organic molecules. Its structure contains a BOC (tert-butyloxycarbonyl) protecting group, which helps to prevent unwanted reactions at specific sites during chemical transformations. Additionally, the vinyloxazolidine group in its structure makes it suitable for use in various organic transformations, such as cycloadditions and cross-coupling reactions. Overall, (R)-N-BOC-2,2-DIMETHYL-4-VINYLOXAZOLIDINE is an important building block in organic synthesis, with diverse applications in the pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 115378-31-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,3,7 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 115378-31:
(8*1)+(7*1)+(6*5)+(5*3)+(4*7)+(3*8)+(2*3)+(1*1)=119
119 % 10 = 9
So 115378-31-9 is a valid CAS Registry Number.

115378-31-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl (4R)-4-ethenyl-2,2-dimethyl-1,3-oxazolidine-3-carboxylate

1.2 Other means of identification

Product number -
Other names (R)-N-Boc-vinylglycinol acetonide

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:115378-31-9 SDS

115378-31-9Relevant articles and documents

Methylenation of aldehydes: Transition metal catalyzed formation of salt-free phosphorus ylides

Lebel, Heandleandne,Paquet, Valeandrie,Proulx, Caroline

, p. 2887 - 2890 (2007/10/03)

A variety of terminal alkenes are produced in excellent yields by the rhodium(I)-catalyzed methylenation of aldehydes using TMSCHN2 and PPh3 [Eq. (1)]. These mild reaction conditions allowed the conversion of enolizable substrates and the chemoselective methylenation of aldehydes over ketones. TMS = trimethylsilyl.

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