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B4856

Diphenylmethanol

Name: Diphenylmethanol
Brand: ALDRICH

99%

Synonym(s):

Benzhydrol, Benzhydryl alcohol, Diphenyl carbinol

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About This Item

Linear Formula:

(C₆H₅)₂CHOH

CAS Number:

91-01-0

Molecular Weight:

184.23

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24891706

EC Number:

202-033-8

Beilstein/REAXYS Number:

1424379

MDL number:

MFCD00004488

Assay:

99%

Form:

powder

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Properties

Quality Level

100

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

Description

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.

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Storage Class

11 - Combustible Solids

wgk

WGK 2

ppe

dust mask type N95 (US), Eyeshields, Gloves

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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)

Discovery of novel tricyclic compounds as squalene synthase inhibitors.

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

Synthesis and biological evaluation of (±)-benzhydrol derivatives as potent non-nucleoside HIV-1 reverse transcriptase inhibitors.

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)

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Global Trade Item Number

SKU	GTIN
B4856-100G	04061833433461
B4856-500G	04061833433478
B4856-5G	04061833433485