Product Name :
2,3,4,5,6-Pentafluorobenzoyl chloride
CAS :
2251-50-5
Molecular Weight:
230.52
Formula:
RIDADR :
NONH for all modes of transport
Symbol :
GHS05
Specification:
| Hazard Statements H314 | RIDADR NONH for all modes of transport | Symbol GHS05 What is the molecular formula of 2,3,4,5,6-Pentafluorobenzoyl chloride? The molecular formula of 2,3,4,5,6-Pentafluorobenzoyl chloride is C7ClF5O. What is the molecular weight of 2,3,4,5,6-Pentafluorobenzoyl chloride? The molecular weight of 2,3,4,5,6-Pentafluorobenzoyl chloride is 230.52 g/mol. What is the IUPAC name of 2,3,4,5,6-Pentafluorobenzoyl chloride? The IUPAC name of 2,3,4,5,6-Pentafluorobenzoyl chloride is 2,3,4,5,6-pentafluorobenzoyl chloride. 1505818-73-4 Chemscene What is the InChI of 2,3,4,5,6-Pentafluorobenzoyl chloride? The InChI of 2,3,4,5,6-Pentafluorobenzoyl chloride is InChI=1S/C7ClF5O/c8-7(14)1-2(9)4(11)6(13)5(12)3(1)10. Buy199105-03-8 What is the InChIKey of 2,3,4,5,6-Pentafluorobenzoyl chloride? The InChIKey of 2,3,4,5,6-Pentafluorobenzoyl chloride is MYHOHFDYWMPGJY-UHFFFAOYSA-N. What is the canonical SMILES of 2,3,4,5,6-Pentafluorobenzoyl chloride? The canonical SMILES of 2,3,4,5,6-Pentafluorobenzoyl chloride is C1(=C(C(=C(C(=C1F)F)F)F)F)C(=O)Cl. What is the CAS number of 2,3,4,5,6-Pentafluorobenzoyl chloride? The CAS number of 2,3,4,5,6-Pentafluorobenzoyl chloride is 2251-50-5. What is the molecular weight of 2,3,4,5,6-Pentafluorobenzoyl chloride according to PubChem? The molecular weight of 2,3,4,5,6-Pentafluorobenzoyl chloride is 230.52 g/mol. What is the XLogP3-AA value of 2,3,4,5,6-Pentafluorobenzoyl chloride? The XLogP3-AA value of 2,3,4,5,6-Pentafluorobenzoyl chloride is 2.9. How many hydrogen bond acceptor counts does 2,3,4,5,6-Pentafluorobenzoyl chloride have? 2,3,4,5,6-Pentafluorobenzoyl chloride has 6 hydrogen bond acceptor counts. Upstream Synthesis Route 1 602-94-8 2251-50-5 Reference: [1]Chinese Chemical Letters,2013,vol. 24,p. 673 – 676[2]Journal of Fluorine Chemistry,2016,vol. 187,p. 15 – 23[3]Russian Journal of Organic Chemistry,2018,vol. 54,p. 1480 – 1485Zh. Org. Khim.,2018,vol. 54,p. 1468 – 1475,8[4]Journal of Fluorine Chemistry,2020,vol. 236[5]Canadian Journal of Chemistry,1972,vol. 50,p. 512 – 520[6]Journal of the Chemical Society,1961,p. 808 – 817[7]Journal of Medicinal Chemistry,1990,vol. 33,p. 1406 – 1413[8]Journal of Organometallic Chemistry,1982,vol. 233,p. 267 – 274[9]Journal of Organic Chemistry,1993,vol. 58,p. 7128 – 7134[10]Pesticide Science,1994,vol. 41,p. 139 – 148[11]Russian Journal of Organic Chemistry,2003,vol. 39,p. 248 – 256[12]Bulletin of the Chemical Society of Japan,2003,vol. 76,p. 1441 – 1446[13]Bioorganic and Medicinal Chemistry Letters,2004,vol. 14,p. 5781 – 5786[14]Journal of Fluorine Chemistry,2005,vol. 126,p. 739 – 743[15]Organic and Biomolecular Chemistry,2006,vol. 4,p. 4370 – 4374[16]Journal of Medicinal Chemistry,2008,vol. 51,p. 4115 – 4121[17]Beilstein Journal of Organic Chemistry,2013,vol. 9,p. 633 – 640[18]Journal of the American Chemical Society,2014,vol. 136,p. 3002 – 3005[19]Asian Journal of Chemistry,2014,vol. 26,p. 2362 – 2364[20]European Journal of Medicinal Chemistry,2017,vol. 128,p. 79 – 87[21]Journal of Fluorine Chemistry,2017,vol. 197,p. 49 – 58[22]Chemical Biology and Drug Design,2017,vol. 90,p. 156 – 161[23]Journal of Medicinal Chemistry,2019,vol. 62,p. 9600 – 9617[24]Patent: CN111233664,2020,A .Location in patent: Paragraph 0027-0029 Downstream Synthesis Route 1 67-56-12251-50-5 36629-42-2 Reference: [1] Journal of Medicinal Chemistry, 2002, vol. 45, # 8, p. 1678 – 1685[2] Journal of Organic Chemistry, 1988, vol. 53, # 14, p. 3321 – 3325[3] Asian Journal of Chemistry, 2014, vol. 26, # 8, p. 2362 – 2364 Downstream Synthesis Route 2 2251-50-5828-73-9 19364-94-4 Reference: [1]Dass, Geetha; Jeyasingh, Vanthana; Kumaresan, Murugesan; Lakshminarayanan, Sudha; Piramuthu, Lakshminarayanan; Selvapalam, Narayanan[Chemical Papers, 2022, vol. 76, # 3, p. 1891 – 1898][2]Chambers,R.D. et al.[Journal of the Chemical Society C: Organic, 1968, p. 1933 – 1937] Downstream Synthesis Route 3 94-97-32251-50-5 76884-11-2 Reference: [1]Journal of Heterocyclic Chemistry,1980,vol. 17,p. 1505 – 1508 * For details of the synthesis route, please refer to the original source to ensure accuracy.
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