B4856
Diphenylmethanol
99%
Synonym(s):
Benzhydrol, Benzhydryl alcohol, Diphenyl carbinol
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Linear Formula:
(C6H5)2CHOH
CAS Number:
Molecular Weight:
184.23
Beilstein:
1424379
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
99%
form
powder
bp
297-298 °C (lit.)
mp
65-67 °C (lit.)
SMILES string
OC(c1ccccc1)c2ccccc2
InChI
1S/C13H12O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13-14H
InChI key
QILSFLSDHQAZET-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Application
Diphenylmethanol is used in the carbene-catalyzed dynamic kinetic resolution of α,α-disubstituted carboxylic esters. It can also be used in the chiral resolution of free-base and Ni(II) porphyrinoid complexes.
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Carbene-Catalyzed Dynamic Kinetic Resolution of Carboxylic Esters.
Chen X, et al.
Journal of the American Chemical Society, 138(23), 7212-7215 (2016)
Helimeric porphyrinoids: stereostructure and chiral resolution of meso-tetraarylmorpholinochlorins.
Bru?ckner C, et al.
Journal of the American Chemical Society, 133(22), 8740-8752 (2011)
Alkylation of alcohols for gas chromatographic analysis by a phase transfer catalysis technique. Evaluation of benzhydrol benzylation in a one-phase system.
H Brink et al.
Acta pharmaceutica Suecica, 16(4), 247-262 (1979-01-01)
Xiao-Dong Ma et al.
Bioorganic & medicinal chemistry, 19(16), 4704-4709 (2011-07-27)
A series of (±)-benzhydrol derivatives featuring the essential sulfonamide group at the para position on the C-ring were synthesized and evaluated for the potential anti-HIV activity in C8166 cells. Most of these analogues demonstrated low concentration inhibitory activity with EC(50)
Masanori Ichikawa et al.
Bioorganic & medicinal chemistry, 20(9), 3072-3093 (2012-04-03)
In the present article, we have reported the design, synthesis, and identification of highly potent benzhydrol derivatives as squalene synthase inhibitors (compound 1). Unfortunately, the in vivo efficacies of the compounds were not enough for acquiring the clinical candidate. We
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service