Key Documents

View All Documentation

362565

Bis(diethylamino)chlorophosphine

Name: Bis(diethylamino)chlorophosphine
Brand: ALDRICH

97%, liquid

Synonym(s):

Chlorobis(diethylamino)phosphine

Select a Size

Change View

About This Item

Linear Formula:

[(C₂H₅)₂N]₂PCl

CAS Number:

685-83-6

Molecular Weight:

210.68

UNSPSC Code:

12352001

PubChem Substance ID:

24862321

NACRES:

NA.22

MDL number:

MFCD00015493

Technical Service

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

Let Us Assist

Properties

Product Name

Bis(diethylamino)chlorophosphine, 97%

assay

97%

form

liquid

reaction suitability

reaction type: Buchwald-Hartwig Cross Coupling Reaction, reaction type: Heck Reaction, reaction type: Hiyama Coupling, reaction type: Negishi Coupling, reaction type: Sonogashira Coupling, reaction type: Stille Coupling, reaction type: Suzuki-Miyaura Coupling

refractive index

n20/D 1.4895 (lit.)

bp

55-57 °C/0.2 mmHg (lit.)

density

1.002 g/mL at 25 °C (lit.)

functional group

phosphine

SMILES string

CCN(CC)P(Cl)N(CC)CC

InChI

1S/C8H20ClN2P/c1-5-10(6-2)12(9)11(7-3)8-4/h5-8H2,1-4H3

InChI key

JVEHJSIFWIIFHM-UHFFFAOYSA-N

Description

pictograms

GHS05

signalword

Danger

hcodes

H314

pcodes

P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363 - P405

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

supp_hazards

EUH014

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

213.8 °F - closed cup

flash_point_c

101 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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

Synthesis and interactive properties of an oligonucleotide with anthraquinone at the sugar fragment.

K Yamana et al.

Bioconjugate chemistry, 1(5), 319-324 (1990-09-01)

The synthesis of a self-complementary oligonucleotide possessing an anthraquinonylmethyl substituent at the designated sugar fragment, 5'-CCU(2'AQ)AGCTAGG (1), is described. The anthraquinonylmethyl group was introduced to 2'-hydroxyl moiety of uridine, which was then converted to the protected phosphorobisdiethylamidite derivative. This reagent

A phosphorbisamidite approach to the synthesis of oligodeoxyribonucleotides and their analogues.