跳转至内容
Merck
CN

145858

1,3-二氰基苯

98%

别名:

间苯二氰, 间苯二甲腈

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:
C6H4(CN)2
化学文摘社编号:
分子量:
128.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-933-7
Beilstein/REAXYS Number:
1072209
MDL number:
Assay:
98%
Form:
liquid
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


Quality Level

assay

98%

form

liquid

mp

163-165 °C (lit.)

functional group

nitrile

SMILES string

N#Cc1cccc(c1)C#N

InChI

1S/C8H4N2/c9-5-7-2-1-3-8(4-7)6-10/h1-4H

InChI key

LAQPNDIUHRHNCV-UHFFFAOYSA-N

Application

1,3-Dicyanobenzene was used in the synthesis of oxazolines and 1,3-bis-(4,4-dimethyl-2-oxazolinyl)benzene.


pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

存储类别

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, 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。

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



Glenn R Masson et al.
The Biochemical journal, 474(11), 1867-1877 (2017-04-07)
Until recently, one of the major limitations of hydrogen/deuterium exchange mass spectrometry (HDX-MS) was the peptide-level resolution afforded by proteolytic digestion. This limitation can be selectively overcome through the use of electron-transfer dissociation to fragment peptides in a manner that
A SIMPLE LARGE SCALE SYNTHESIS OF 1, 3-BIS-(4, 4-DIMETHYL-2-OXAZOLINYL) BENZENE 1*.
Button KM, et al.
Synthetic Communications, 32(3), 363-368 (2002)
Luo Mei et al.
Journal of combinatorial chemistry, 11(2), 220-227 (2009-01-14)
A class of modular oxazolines and their derivatives 1-5 were synthesized with moderate to excellent yields using a simple one-pot method; 4 x 3 bis-oxazolines were obtained, as expected, from each of the three reactions of 1,4-dicyanobenzene, 1,3-dicyanobenzene, and 1,2-dicyanobenzene



全球贸易项目编号

货号GTIN
145858-5G04061838736499
145858-250G04061832106090