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Merck
CN

187518

2,6-二氯苯甲酰氯

99%

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关于此项目

线性分子式:
Cl2C6H3COCl
化学文摘社编号:
分子量:
209.46
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39050513
UNSPSC Code:
12352100
EC Number:
225-102-4
MDL number:
Beilstein/REAXYS Number:
639531
Assay:
99%
Form:
liquid
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Quality Level

assay

99%

form

liquid

refractive index

n20/D 1.560 (lit.)

bp

142-143 °C/21 mmHg (lit.)

mp

15-17 °C

density

1.462 g/mL at 25 °C (lit.)

functional group

acyl chloride, chloro

SMILES string

ClC(=O)c1c(Cl)cccc1Cl

InChI

1S/C7H3Cl3O/c8-4-2-1-3-5(9)6(4)7(10)11/h1-3H

InChI key

JBLIDPPHFGWTKU-UHFFFAOYSA-N

General description

2,6-Dichlorobenzoyl chloride participates in esterification of (fluoren-9-ylmethoxy)carbonyl (Fmoc)-amino acids to 4-alkoxybenzyl alcohol polystyrene.

Application

2,6-Dichlorobenzoyl chloride was used:
  • in substrate activity screening method for the rapid development of novel substrates and their conversion into non-peptidic inhibitors of Cys and Ser proteases
  • in the synthesis of 1-acyliridoles
  • in enantiocontrolled total synthesis of (-)-aspicilin


pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 1

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

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



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Morphine recognition by a porphyrin-cyclocholate molecular bowl.
Bonar-Law RP, et al.
Journal of the Chemical Society. Chemical Communications, 5, 456-458 (1993)
An improved method for anchoring of 9-fluorenylmethoxycarbonyl-amino acids to 4-alkoxybenzyl alcohol resins.
Sieber, P.
Tetrahedron Letters, 28(49), 6147-6150 (1987)
Sensitisation to dichlorobenzoyl chloride.
J De Boer et al.
Contact dermatitis, 18(2), 116-117 (1988-02-01)



全球贸易项目编号

货号GTIN
187518-10G04061838758590
187518-50G04061837376214