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Merck
CN

259772

氯磺酰基乙酰氯

95%

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线性分子式:
ClSO2CH2COCl
化学文摘社编号:
分子量:
177.01
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
223-693-3
MDL number:
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产品名称

氯磺酰基乙酰氯, 95%

InChI key

MCFSNYMQISXQTF-UHFFFAOYSA-N

InChI

1S/C2H2Cl2O3S/c3-2(5)1-8(4,6)7/h1H2

SMILES string

ClC(=O)CS(Cl)(=O)=O

vapor pressure

0.06 mmHg ( 20 °C)

assay

95%

form

liquid

refractive index

n20/D 1.493 (lit.)

bp

71-72 °C/1 mmHg (lit.)

density

1.669 g/mL at 25 °C (lit.)

Quality Level

Application

Chlorosulfonylacetyl chloride has been used in:
  • preparation of novel tricyclic benzothiazolo [2,3-c] thiadiazine antagonists of the platelet ADP receptor
  • N-terminal derivatization of peptides in rapid determination of peptide or protein sequences by matrix-assisted laser desorption ionization mass spectrometry

pictograms

CorrosionExclamation mark

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

supp_hazards

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 3

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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R M Scarborough et al.
Bioorganic & medicinal chemistry letters, 11(14), 1805-1808 (2001-07-19)
Novel non-nucleoside tricyclic platelet ADP receptor (P2Y(12)) antagonists have been discovered that bind reversibly and with high affinity to the platelet receptor. Condensation of various 2-aminobenzothiazoles with chlorosulfonylacetyl chloride affords these novel tricyclic heterocycles, which are novel and unpredicted products
T Keough et al.
Proceedings of the National Academy of Sciences of the United States of America, 96(13), 7131-7136 (1999-06-23)
A method has been developed for de novo peptide sequencing using matrix-assisted laser desorption ionization mass spectrometry. This method will facilitate biological studies that require rapid determination of peptide or protein sequences, e.g., determination of posttranslational modifications, identification of active

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