主要文件

查看所有文档

359505

7-甲基-1,5,7-三氮杂二环[4.4.0]癸-5-烯

Name: 7-甲基-1,5,7-三氮杂二环[4.4.0]癸-5-烯
Brand: ALDRICH

98%

别名:

1,3,4,6,7,8-六氢-1-甲基-2H-嘧啶并[1,2-a]嘧啶, MTBD

登录查看组织和合同定价。

选择尺寸

变更视图

关于此项目

经验公式（希尔记法）:

C₈H₁₅N₃

化学文摘社编号:

84030-20-6

分子量:

153.22

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24862083

EC Number:

281-791-1

Beilstein/REAXYS Number:

7635759

MDL number:

MFCD00043004

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

属性

assay

98%

form

liquid

refractive index

n20/D 1.537 (lit.)

bp

75-79 °C/0.1 mmHg (lit.)

density

1.067 g/mL at 25 °C (lit.)

SMILES string

CN1CCCN2CCCN=C12

InChI

1S/C8H15N3/c1-10-5-3-7-11-6-2-4-9-8(10)11/h2-7H2,1H3

InChI key

OEBXWWBYZJNKRK-UHFFFAOYSA-N

说明

General description

7-甲基-1,5,7-三氮杂二环[4.4.0]癸-5-烯是一种可溶性胺碱。它与4-硝基苯基[双(二乙基磺酰基)]甲烷和苯基[双(二乙基磺酰基)]甲烷形成1:1配合物，并且已通过FT-IR、¹H NMR和PM5半经验方法研究了它们的结构。已经研究了7-甲基-1,5,7-三氮杂二环[4.4.0]癸-5-烯对菜籽油与甲醇的酯交换反应的催化性能。

Application

7-甲基-1,5,7-三氮杂二环[4.4.0]癸-5-烯可用于微波促进的、钯催化的与芳基/杂芳基九氟磺酸盐和胺的C-N键形成反应。它可以作为强碱，用于研究多足配体溶剂、三(氧杂烷基)苯基硅烷和三(氧杂烷基)磷酸酯。

pictograms

GHS05

signalword

Danger

hcodes

H314

pcodes

P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363 - P405

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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

商品

Deoxyfluorination with 2-Pyridinesulfonyl Fluoride (PyFluor)

The prevalence of organofluorine compounds in industry and drug design necessitates the ability to introduce C–F bonds to molecules.

Spectroscopic studies of the 1: 1 complexes of 4-nitrophenyl [bis (ethylsulfonyl)] methane and phenyl [bis (ethylsulfonyl)] methane with 7-methyl-1, 5, 7-triazabicyclo [4.4. 0] dec-5-ene and 1, 5, 7-triazabicyclo [4.4. 0] dec-5-ene.

Huczynski A, et al.

Journal of Molecular Structure, 841(1), 133-136 (2007)

Expedited palladium-catalyzed amination of aryl nonaflates through the use of microwave-irradiation and soluble organic amine bases.

Rachel E Tundel et al.

The Journal of organic chemistry, 71(1), 430-433 (2006-01-04)

[reaction: see text] Microwave-assisted, palladium-catalyzed C-N bond-forming reactions with aryl/heteroaryl nonaflates and amines using the soluble amine bases DBU (1,8-diazabicyclo[5.4.0]undec-7-ene) or MTBD (7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene) and ligands (1-3) resulted in good to excellent yields (71-99%) of arylamines in short reaction times (1-45

Transesterification of vegetable oils: a review.

Schuchardt U, et al.

Journal of the Brazilian Chemical Society, 9(3), 199-210 (1998)

查看所有相关文献

全球贸易项目编号

货号	GTIN
359505-1ML	04061838053848
359505-5ML	04061831813272