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Merck
CN

391220

2-Chloro-1,3,2-dioxaphospholane

97%, liquid

Synonym(s):

Cyclic ethylene chlorophosphite, Cyclic ethylene phosphorochloridite, Ethylene chlorophosphite, Ethylene glycol chlorophosphite

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About This Item

Empirical Formula (Hill Notation):
C2H4ClO2P
CAS Number:
Molecular Weight:
126.48
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
EC Number:
212-499-4
MDL number:
Beilstein/REAXYS Number:
506179
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Product Name

2-Chloro-1,3,2-dioxaphospholane, 97%

Quality Level

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, reagent type: ligand

refractive index

n20/D 1.489 (lit.)

bp

62 °C/20 mmHg (lit.)

density

1.422 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

ClP1OCCO1

InChI

1S/C2H4ClO2P/c3-6-4-1-2-5-6/h1-2H2

InChI key

OLSFRDLMFAOSIA-UHFFFAOYSA-N

Application

Phosphitylating agent used in the synthesis of phosphocholines and spirophosphoranes.


pictograms

CorrosionExclamation mark

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

supp_hazards

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

186.8 °F - closed cup

flash_point_c

86 °C - closed cup

ppe

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



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Tetrahedron Letters, 35, 5783-5783 (1994)
Rec. Trav. Chim., 113, 293-293 (1994)
Xue Wan et al.
Biomolecules, 9(12) (2019-12-11)
Effective valorization of lignin is crucial to achieve a sustainable, economic and competitive biorefinery of lignocellulosic biomass. In this work, an integrated process was proposed based on a concentrated phosphoric acid plus hydrogen peroxide (PHP) pretreatment to simultaneously facilitate cellulose



Global Trade Item Number

SKUGTIN
391220-5ML04061838047595