4-Chlorobenzhydrol, 98%

Name: 4-Chlorobenzhydrol, 98% | 119-56-2
Brand: J&K Chemical
SKU: JK166211_100_G
Price: 120.5 USD
Availability: InStock

Cat. No JK166211_100_G

Vendor: J&K Chemical

Product Information

Product Name

4-Chlorobenzhydrol, 98%

Brand Name

J&K

Product Number

166211

CAS

119-56-2

Molecular Formula

C13H11ClO

Molecular Weight

218.68

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

4-Chlorodiphenylmethanol

PubChem CID

8401

IUPAC Name

(4-chlorophenyl)-phenylmethanol

InChI Key

AJYOOHCNOXWTKJ-UHFFFAOYSA-N

SMILES

C1=CC=C(C=C1)C(C2=CC=C(C=C2)Cl)O

Properties

Melting Point

58-60

References Data Source From Pubchem

Sustainable and Validated Spectrophotometric Methods for the Analysis of a Ternary Mixture of Cloperastine Fendizoate, Its Degradant, and Methylparaben

Publication Name: Journal of Analytical Chemistry

Publication Date: 2026-01

DOI: 10.1134/s1061934825701382

Facile one-pot preparation of chiral metal–organic framework L-His-ZIF-67@SiO2 composite for HPLC enantioseparation

Publication Name: Microchimica Acta

Publication Date: 2025-09-28

DOI: 10.1007/s00604-025-07558-3

Reactions with Alkynes and Alcohols

Publication Name: Science of Synthesis

Publication Date: 2025

Asymmetric catalytic synthesis of chiral covalent organic framework composite (S)-DTP-COF@SiO2 for HPLC enantioseparations by normal-phase and reversed-phase chromatographic modes

Publication Name: Microchimica Acta

Publication Date: 2024-07-03

DOI: 10.1007/s00604-024-06524-9

Coupling metal and whole-cell catalysis to synthesize chiral alcohols

Publication Name: Bioresources and Bioprocessing

Publication Date: 2022-07-08

DOI: 10.1186/s40643-022-00560-0

4-Chlorobenzhydrol, 98%

Product Information

General Information

Properties

References Data Source From Pubchem

Sustainable and Validated Spectrophotometric Methods for the Analysis of a Ternary Mixture of Cloperastine Fendizoate, Its Degradant, and Methylparaben

Facile one-pot preparation of chiral metal–organic framework L-His-ZIF-67@SiO2 composite for HPLC enantioseparation

Reactions with Alkynes and Alcohols

Asymmetric catalytic synthesis of chiral covalent organic framework composite (S)-DTP-COF@SiO2 for HPLC enantioseparations by normal-phase and reversed-phase chromatographic modes

Coupling metal and whole-cell catalysis to synthesize chiral alcohols