2,4,6-Trichlorobenzyl alcohol - CAS 217479-60-2
Catalog: |
BB017133 |
Product Name: |
2,4,6-Trichlorobenzyl alcohol |
CAS: |
217479-60-2 |
Synonyms: |
(2,4,6-trichlorophenyl)methanol |
IUPAC Name: | (2,4,6-trichlorophenyl)methanol |
Description: | 2,4,6-Trichlorobenzyl alcohol (CAS# 217479-60-2) is an intermediate in the synthesis of 1,3,5-Trichloro-2-methylbenzene (T774363). 1,3,5-Trichloro-2-methylbenzene can be used as reactant/reagent in hydrodechlorination process and catalysts for the production of 2,6-dichlorotoluene from polychlorotoluene-containing mixtures. Also, it is derived from 2,4,6-Trichlorobenzoic Acid (T774715), which is a possible degradation intermediate of Polychlorinated Biphenyls (PCBs) in contaminated soil, suggesting the occurrence of microbial transformation processes over time. |
Molecular Weight: | 211.47 |
Molecular Formula: | C7H5Cl3O |
Canonical SMILES: | C1=C(C=C(C(=C1Cl)CO)Cl)Cl |
InChI: | InChI=1S/C7H5Cl3O/c8-4-1-6(9)5(3-11)7(10)2-4/h1-2,11H,3H2 |
InChI Key: | WKJWKKDGJLKFER-UHFFFAOYSA-N |
Boiling Point: | 299.4 ℃ at 760 mmHg |
Melting Point: | 98-101 ℃ (lit.) |
Purity: | 95 % |
Density: | 1.52 g/cm3 |
MDL: | MFCD03093891 |
LogP: | 3.13910 |
GHS Hazard Statement: | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
WO-2020141195-A1 | Fluorine-containing compounds for use as nucleophilic reagents for transferring functional groups onto high value organic compounds | 20190103 |
US-2020283562-A1 | Application of mannich base in flame-retardant polyurethane material | 20180917 |
US-2020283573-A1 | Flame-retardant polyether polyol as well as preparation method and application thereof | 20180917 |
AU-2013276617-B9 | New diazaspirocycloalkane and azaspirocycloalkane | 20120613 |
EP-2861566-B1 | New diazaspirocycloalkane and azaspirocycloalkane | 20120613 |
PMID | Publication Date | Title | Journal |
15844893 | 20050428 | Catalytic enantioselective sulfinyl transfer using cinchona alkaloid catalysts | Organic letters |
Complexity: | 119 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 209.940598 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 209.940598 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 20.2 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 2.9 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Oxygen Compounds
Customers Also Viewed
-
[1271-47-2]
Ethynylferrocene
-
[120739-62-0]
N-[(6-Chloropyridin-3-yl)methyl]-N-methylamine
-
[132182-92-4]
Pentane, 1,1,1,2,2,3,4,5,5,5-decafluoro-3-methoxy-4-(trifluoromethyl)-
-
[57166-92-4]
Methylenediamine dihydrochloride
-
[5518-18-3]
N-[2-(hexadecanoylamino)ethyl]hexadecanamide
-
[35153-16-3]
(Z)-10-Tetradecenyl Acetate
INDUSTRY LEADERS TRUST OUR PRODUCTS