Key Documents

View All Documentation

B18200

Benzyl carbamate

Name: Benzyl carbamate
Brand: ALDRICH

99%

Select a Size

Change View

About This Item

Linear Formula:

NH₂COOCH₂C₆H₅

CAS Number:

621-84-1

Molecular Weight:

151.16

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24891616

EC Number:

210-710-4

Beilstein/REAXYS Number:

1865635

MDL number:

MFCD00007965

Assay:

99%

Form:

flakes

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

Quality Level

200

assay

99%

form

flakes

mp

86-89 °C (lit.)

SMILES string

NC(=O)OCc1ccccc1

InChI

1S/C8H9NO2/c9-8(10)11-6-7-4-2-1-3-5-7/h1-5H,6H2,(H2,9,10)

InChI key

PUJDIJCNWFYVJX-UHFFFAOYSA-N

Description

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Site-selective chemical modification of chymotrypsin using peptidyl derivatives bearing optically active diphenyl 1-amino-2-phenylethylphosphonate: Stereochemical effect of the diphenyl phosphonate moiety.

Shin Ono et al.

Biopolymers, 106(4), 521-530 (2015-12-01)

Diphenyl (α-aminoalkyl)phosphonates act as mechanism-based inhibitors against serine proteases by forming a covalent bond with the hydroxy group of the active center Ser residue. Because the covalent bond was found to be broken and replaced by 2-pyridinaldoxime methiodide (2PAM), we

Mixed alkyl aryl phosphonate esters as quenched fluorescent activity-based probes for serine proteases.

Sevnur Serim et al.

Organic & biomolecular chemistry, 13(8), 2293-2299 (2015-01-03)

Activity-based probes (ABPs) are powerful tools for the analysis of active enzyme species in whole proteomes, cells or animals. Quenched fluorescent ABPs (qABPs) can be applied for real time imaging, allowing the visualization of dynamic enzyme activation by fluorescent microscopy.

Global Trade Item Number

SKU	GTIN
B18200-100G	04061838352446
B18200-25G	04061833426494