(R)-(+)-3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, 95%

Name: (R)-(+)-3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, 95% | 95715-87-0
Brand: J&K Chemical
SKU: JK214344_1_G
Price: 322.0 USD
Availability: OutOfStock

Cat. No JK214344_1_G

Vendor: J&K Chemical

Product Information

Product Name

(R)-(+)-3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, 95%

Brand Name

J&K

Product Number

214344

CAS

95715-87-0

Molecular Formula

C11H19NO4

Molecular Weight

229.27

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

tert-Butyl (R)-(+)-4-formyl-2,2-dimethyloxazolidine-3-carboxylate

PubChem CID

178792

IUPAC Name

tert-butyl (4R)-4-formyl-2,2-dimethyl-1,3-oxazolidine-3-carboxylate

InChI Key

PNJXYVJNOCLJLJ-QMMMGPOBSA-N

SMILES

CC1(N(C@H(CO1)C=O)C(=O)OC(C)(C)C)C

Properties

Density

1.06

Boiling Point

Flash Point

102

n20D

1.4450-1.4550

Optical Activity

+87°to +99° (C=1, CHCl3)

Safety Information

GHS Symbols

Signal Word

Warning

Hazard Statement

H315

H319

H335

Precautionary Statement

P280

P321

P261

P271

P319

P405

P501

P302+P352

P332+P317

P362+P364

P264+P265

P305+P351+P338

P337+P317

P304+P340

P403+P233

References Data Source From Pubchem

Strategies for the Synthesis of Selenocysteine Derivatives

Publication Name: Synthesis

Publication Date: 2021-10-06

DOI: 10.1055/a-1588-9763

Stereoselective Synthesis of (4S,5S)-5-Vinyloxazolidin-2-one-4-carboxylate as a β-Vinylserine Synthetic Equivalent by Vinyl Grignard Addition to an N-Tosyl Version of Garner’s Aldehyde

Publication Name: Synlett : accounts and rapid communications in synthetic organic chemistry

Publication Date: 2021-01-08

DOI: 10.1055/a-1308-0370

Homologation Reactions of α-Oxy Boronate Esters

Publication Name: Science of Synthesis

Publication Date: 2019

Recent Advances in the Total Synthesis of Clavaminols

Publication Name: Synthesis

Publication Date: 2018-10-18

DOI: 10.1055/s-0037-1610305

Deprotonative Construction of a Carbon–Carbon Single Bond by Addition to a C=X Bond

Publication Name: Science of Synthesis

Publication Date: 2017

(R)-(+)-3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, 95%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Strategies for the Synthesis of Selenocysteine Derivatives

Stereoselective Synthesis of (4S,5S)-5-Vinyloxazolidin-2-one-4-carboxylate as a β-Vinylserine Synthetic Equivalent by Vinyl Grignard Addition to an N-Tosyl Version of Garner’s Aldehyde

Homologation Reactions of α-Oxy Boronate Esters

Recent Advances in the Total Synthesis of Clavaminols

Deprotonative Construction of a Carbon–Carbon Single Bond by Addition to a C=X Bond