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Merck
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文件

409235

Sigma-Aldrich

2-甲基-1-(三甲基硅氧基)-1-丙烯

99%

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About This Item

线性分子式:
(CH3)2C=CHOSi(CH3)3
CAS号:
6651-34-9
分子量:
144.29
MDL號碼:
MFCD00192331
分類程式碼代碼:
12352100
PubChem物質ID:
24865629

化驗

99%

形狀

liquid

折射率

n20/D 1.409 (lit.)

bp

114-116 °C/650 mmHg (lit.)

密度

0.785 g/mL at 25 °C (lit.)

SMILES 字串

C\C(C)=C\O[Si](C)(C)C

InChI

1S/C7H16OSi/c1-7(2)6-8-9(3,4)5/h6H,1-5H3

InChI 密鑰

KZVPFSJPLBOVLO-UHFFFAOYSA-N

一般說明

2-Methyl-1-(trimethylsilyloxy)-1-propene is an enol ether.

應用

2-Methyl-1-(trimethylsilyloxy)-1-propene may be used as reagent in the direct conversion of α-amino acids into β-amino aldehydes.

象形圖

FlameExclamation mark
GHS02,GHS07

訊號詞

Danger

危險分類

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

3 - Flammable liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

57.2 °F - closed cup

閃點（°C）

14 °C - closed cup

個人防護裝備

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

分析证书(COA)

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L Nassi et al.
Mutation research, 198(1), 53-60 (1988-03-01)
Generation of triplet ketones, either chemically through thermal decomposition of 3-hydroxymethyl-3,4,4-trimethyl-1,2-dioxetane and 3-[N-(pyridino)carbamoyl]methyl-3,4,4-trimethyl-1,2-dioxetane++ + or enzymatically via the aerobic oxidation of isobutyraldehyde trimethylsilyl enol ether catalyzed by horse-radish peroxidase, triggers the SOS function sfiA in E. coli. Although the observed
Carlos J Saavedra et al.
Organic & biomolecular chemistry, 10(22), 4448-4461 (2012-05-05)
A direct method for the transformation of α-amino acids into β-amino aldehydes was developed, and applied to the modification of the C-terminal residue of peptides. The method takes place in good yields and under mild conditions. The application of this
G Cilento et al.
Toxicology letters, 67(1-3), 17-28 (1993-04-01)
Selected enzymatic systems can efficiently produce a product in the electronically excited triplet state. Earlier, only the formation of electronically excited singlet species was known. The formation of triplet species has been demonstrated with both normal substrates/metabolites and with xenobiotics

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