N-(tert-Butoxycarbonyl)-2-aminoacetonitrile, 97%

Name: N-(tert-Butoxycarbonyl)-2-aminoacetonitrile, 97% | 85363-04-8
Brand: J&K Chemical
SKU: JK572422_1_G
Price: 4.07 USD
Availability: OutOfStock

Cat. No JK572422_1_G

Vendor: J&K Chemical

Product Information

Product Name

N-(tert-Butoxycarbonyl)-2-aminoacetonitrile, 97%

Brand Name

J&K

Product Number

572422

CAS

85363-04-8

Molecular Formula

C7H12N2O2

Molecular Weight

156.18

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

2-(Boc-amino)acetonitrile
tert-Butyl (cyanomethyl)carbamate

PubChem CID

545844

IUPAC Name

tert-butyl N-(cyanomethyl)carbamate

InChI Key

SMZKPZXYDDZDJG-UHFFFAOYSA-N

SMILES

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

Properties

Melting Point

53-57

Boiling Point

186

Flash Point

113

Safety Information

Storage Condition

Store at 2-8℃

References Data Source From Pubchem

Synthesis of Tetrazines by Ring Construction with Formation of C—N Bonds

Publication Name: Science of Synthesis

Publication Date: 2021

Decarboxylative Cyanation Reaction

Publication Name: Science of Synthesis

Publication Date: 2018

Modifications of the Classical Pinner Method (via Thioimidates)

Publication Name: Science of Synthesis

Publication Date: 2005

(tert-Butoxycarbonylamino)acetonitrile

Publication Name: Acta Crystallographica Section C Crystal Structure Communications

Publication Date: 1997-07-15

DOI: 10.1107/s0108270197002795

CCDC 128795: Experimental Crystal Structure Determination

Publication Date: 1997

DOI: 10.5517/cc4b0p4

N-(tert-Butoxycarbonyl)-2-aminoacetonitrile, 97%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Synthesis of Tetrazines by Ring Construction with Formation of C—N Bonds

Decarboxylative Cyanation Reaction

Modifications of the Classical Pinner Method (via Thioimidates)

(tert-Butoxycarbonylamino)acetonitrile

CCDC 128795: Experimental Crystal Structure Determination