跳转至内容
Merck
所有图片(1)

Key Documents

更多文件

28440

Sigma-Aldrich

氰乙酸叔丁酯

≥97.0% (GC)

登录查看公司和协议定价
所有图片(1)

About This Item

线性分子式:
NCCH2COOC(CH3)3
CAS号:
1116-98-9
分子量:
141.17
Beilstein:
1755933
EC號碼:
214-243-7
MDL號碼:
MFCD00001938
分類程式碼代碼:
12352100
PubChem物質ID:
57648301
NACRES:
NA.22

品質等級

100

化驗

≥97.0% (GC)

折射率

n20/D 1.420

bp

40-42 °C/0.1 mmHg (lit.)

密度

0.988 g/mL at 20 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

CC(C)(C)OC(=O)CC#N

InChI

1S/C7H11NO2/c1-7(2,3)10-6(9)4-5-8/h4H2,1-3H3

InChI 密鑰

BFNYNEMRWHFIMR-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

相关类别

一般說明

tert-Butyl cyanoacetate undergoes functionalization and decarboxylation to form 3-amino-4-alkyl isoquinolines.

應用

tert-Butyl cyanoacetate was used in the synthesis of vinylogous urea.

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

244.4 °F - closed cup

閃點（°C）

118 °C - closed cup

個人防護裝備

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

分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ （Lot或Batch）字后找到。

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

Barry B Snider et al.
Organic letters, 7(20), 4519-4522 (2005-09-24)
[reaction: see text] Addition of the enolate of tert-butyl acetate to cyanamide methyl ester 17 followed by treatment with LHMDS afforded vinylogous urea 19 in 27% yield. Vinylogous urea 19 was also obtained from 37 and tert-butyl cyanoacetate in 50%
Ben S Pilgrim et al.
Organic letters, 15(24), 6190-6193 (2013-11-21)
A methyl ketone, an aryl bromide, an electrophile, and ammonium chloride were combined in a four-component, three-step, and one-pot coupling procedure to furnish substituted isoquinolines in overall yields of up to 80%. This protocol utilizes the palladium catalyzed α-arylation reaction

我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门