tert-Butyl carbamate, 98%

Name: tert-Butyl carbamate, 98% | 4248-19-5
Brand: J&K Chemical
SKU: JK248658_25_G
Price: 69.3 USD
Availability: OutOfStock

Cat. No JK248658_25_G

Vendor: J&K Chemical

Product Information

Product Name

tert-Butyl carbamate, 98%

Brand Name

J&K

Product Number

248658

CAS

4248-19-5

Molecular Formula

C5H11NO2

Molecular Weight

117.15

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

Boc-amide

PubChem CID

77922

IUPAC Name

tert-butyl carbamate

InChI Key

LFKDJXLFVYVEFG-UHFFFAOYSA-N

SMILES

CC(C)(C)OC(=O)N

Properties

Melting Point

105-108

Safety Information

Precautionary Statement

P262

References Data Source From Pubchem

Harnessing thia-Rh-carbenes for the enantioselective synthesis of chiral α,α-diheteroatomic carboxylic acids

Publication Name: Nature Catalysis

Publication Date: 2026-02-06

DOI: 10.1038/s41929-026-01481-3

Concerted 1,3-migration through regiodivergent consecutive 1,2-rearrangements using palladium catalysis

Publication Name: Nature Synthesis

Publication Date: 2026-01-30

DOI: 10.1038/s44160-025-00979-1

New structural scaffold discovery via fragment-based drug design: Hydroxymethyl indazole derivatives as XOR/URAT1 dual inhibitors

Publication Name: Medicinal Chemistry Research

Publication Date: 2025-11-26

DOI: 10.1007/s00044-025-03505-2

Alkynylcarbenes: generation, properties, and application in organic synthesis

Publication Name: Russian Chemical Bulletin

Publication Date: 2025-06

DOI: 10.1007/s11172-024-4648-1

Click Chemistry: An Outstanding Approach for Tuning Natural Products Bioactivities

Publication Name: Revista Brasileira de Farmacognosia

Publication Date: 2025-05-14

DOI: 10.1007/s43450-025-00648-6

tert-Butyl carbamate, 98%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Harnessing thia-Rh-carbenes for the enantioselective synthesis of chiral α,α-diheteroatomic carboxylic acids

Concerted 1,3-migration through regiodivergent consecutive 1,2-rearrangements using palladium catalysis

New structural scaffold discovery via fragment-based drug design: Hydroxymethyl indazole derivatives as XOR/URAT1 dual inhibitors

Alkynylcarbenes: generation, properties, and application in organic synthesis

Click Chemistry: An Outstanding Approach for Tuning Natural Products Bioactivities