4-Chlorobenzyl alcohol - CAS 873-76-7
Catalog: |
BB038414 |
Product Name: |
4-Chlorobenzyl alcohol |
CAS: |
873-76-7 |
Synonyms: |
(4-chlorophenyl)methanol |
IUPAC Name: | (4-chlorophenyl)methanol |
Description: | 4-Chlorobenzyl Alcohol has been used as a reactant in the preparation of p38 kinase inhibitors. |
Molecular Weight: | 142.58 |
Molecular Formula: | C7H7ClO |
Canonical SMILES: | C1=CC(=CC=C1CO)Cl |
InChI: | InChI=1S/C7H7ClO/c8-7-3-1-6(5-9)2-4-7/h1-4,9H,5H2 |
InChI Key: | PTHGDVCPCZKZKR-UHFFFAOYSA-N |
Boiling Point: | 234 °C |
Melting Point: | 69-72 °C |
Purity: | 95 % |
Density: | 1.237 g/cm3 |
Appearance: | Almost white powder |
Storage: | Keep away from sources of ignition. Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances. |
MDL: | MFCD00004652 |
LogP: | 1.83230 |
Publication Number | Title | Priority Date |
CN-113461510-A | Aromatic acid compound and preparation method thereof | 20210804 |
CN-113477183-A | Reaction kettle for p-chlorobenzyl chloride production and production process of p-chlorobenzyl chloride | 20210705 |
CN-113480394-A | Green synthesis method of alkylene fluorene | 20210705 |
CN-113354675-A | Preparation method of 4-hydroxymethyl phenylboronic acid | 20210701 |
CN-113354525-A | Method for preparing carbonyl compound by oxidizing alcohol | 20210529 |
PMID | Publication Date | Title | Journal |
21184141 | 20110901 | A novel metabolic pathway for biodegradation of DDT by the white rot fungi, Phlebia lindtneri and Phlebia brevispora | Biodegradation |
20688518 | 20100901 | S-benzylisothiourea derivatives as small-molecule inhibitors of indoleamine-2,3-dioxygenase | Bioorganic & medicinal chemistry letters |
19115293 | 20090101 | Hetero-seeding and solid mixture to obtain new crystalline forms | Chemistry (Weinheim an der Bergstrasse, Germany) |
18682861 | 20080828 | Oxidation of p-chlorotoluene and cyclohexene catalysed by polymer-anchored oxovanadium(IV) and copper(II) complexes of amino acid derived tridentate ligands | Dalton transactions (Cambridge, England : 2003) |
16528513 | 20060901 | Metabolism of 4,4'-dichlorobiphenyl by white-rot fungi Phanerochaete chrysosporium and Phanerochaete sp. MZ142 | Applied microbiology and biotechnology |
Complexity: | 77 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 142.0185425 |
Formal Charge: | 0 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 142.0185425 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 20.2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 2 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Alcohols and Derivatives
Oxygen Compounds
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS