195995
2-Thiopheneacetyl chloride
98%
Synonym(s):
2-Thienylacetyl chloride
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About This Item
Empirical Formula (Hill Notation):
C6H5ClOS
CAS Number:
Molecular Weight:
160.62
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
254-290-0
Beilstein/REAXYS Number:
114547
MDL number:
Assay:
98%
Form:
liquid
InChI key
AJYXPNIENRLELY-UHFFFAOYSA-N
InChI
1S/C6H5ClOS/c7-6(8)4-5-2-1-3-9-5/h1-3H,4H2
SMILES string
ClC(=O)Cc1cccs1
vapor pressure
4 mmHg ( 83 °C)
assay
98%
form
liquid
Quality Level
bp
105-106 °C/22 mmHg (lit.), 130-135 °C/90 mmHg (lit.)
density
1.303 g/mL at 25 °C (lit.)
functional group
acyl chloride
storage temp.
2-8°C
Related Categories
Application
2-Thiopheneacetyl chloride was used in the synthesis of:
- (S)-ethyl-1-(2-thiopheneacetyl)-3-piperidinecarboxylate, nipecotate-containing immunopotentiator
- 5-fluorouracil-cephalosporin prodrug
- series of new N,N′-di(thiopheneacetyl)diamines derivatives
- 6-β-(thiophen-2′-yl)acetamidomorphine
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
215.6 °F - closed cup
flash_point_c
102 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
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Synthesis and Biological Evaluation of N, N'-di (thiopheneacetyl) diamines Series as Antitubercular Agents.
Nora de Souza MV, et al.
Phosphorus, Sulfur, and Silicon and the Related Elements, 183(12), 2990-2997 (2008)
Development of an efficient synthesis for a nipecotate-containing immunopotentiator.
Moher ED, et al.
Organic Process Research & Development, 8(4), 593-596 (2004)
James M Macdougall et al.
Bioorganic & medicinal chemistry, 12(22), 5983-5990 (2004-10-23)
A series of 6-beta-arylamidomorphines was synthesized and biologically evaluated. Various aryl substituents were introduced into the arylamidomorphines to examine substituent structure-activity relationships. Competition binding assays showed that compounds 10a-h bound to the mu opioid receptor with high affinity (0.2-0.6 nM).
Ryan M Phelan et al.
Bioorganic & medicinal chemistry letters, 19(4), 1261-1263 (2009-01-27)
An efficient synthesis of a 5-fluorouracil-cephalosporin prodrug is described for use against colorectal and other cancers in antibody and gene-directed therapies. The compound shows stability in aqueous media until specifically activated by beta-lactamase (betaL). The kinetic parameters of the 5-fluorouracil-cephalosporin
Radoslaw Laufer et al.
Bioorganic & medicinal chemistry, 22(17), 4968-4997 (2014-07-22)
TTK kinase was identified by in-house siRNA screen and pursued as a tractable, novel target for cancer treatment. A screening campaign and systematic optimization, supported by computer modeling led to an indazole core with key sulfamoylphenyl and acetamido moieties at
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