主要文件

查看所有文档

B4856

二苯甲醇

Name: 二苯甲醇
Brand: ALDRICH

99%

别名:

α-苯基苯甲醇, 二苯基甲醇, 苯甲醇

登录查看组织和合同定价。

选择尺寸

变更视图

关于此项目

线性分子式:

(C₆H₅)₂CHOH

化学文摘社编号:

91-01-0

分子量:

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

技术服务

需要帮助？我们经验丰富的科学家团队随时乐意为您服务。

让我们为您提供帮助

属性

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

说明

Application

二苯基甲醇用于卡宾催化的α，α-二取代羧酸酯的动态动力学拆分。也可用于游离碱和 Ni (II) 卟啉配合物的手性拆分。

Still not finding the right product?

Explore all of our products under 二苯甲醇

存储类别

11 - Combustible Solids

wgk

WGK 2

ppe

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本？

如果您需要特殊版本，可通过批号或批次号查找具体证书。

搜索COA

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

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)

查看所有相关文献

全球贸易项目编号

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