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Merck
CN

P49104

Sigma-Aldrich

胡椒醛

99%

别名:

1,3-苯并二氧戊环-5-甲醛, 3,4-(亚甲二氧基)苯甲醛, 天芥菜醛

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关于此项目

经验公式(希尔记法):
C8H6O3
化学文摘社编号:
分子量:
150.13
Beilstein:
131691
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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蒸汽压

1 mmHg ( 87 °C)

质量水平

方案

99%

表单

solid

沸点

264 °C (lit.)

mp

35-39 °C (lit.)

SMILES字符串

[H]C(=O)c1ccc2OCOc2c1

InChI

1S/C8H6O3/c9-4-6-1-2-7-8(3-6)11-5-10-7/h1-4H,5H2

InChI key

SATCULPHIDQDRE-UHFFFAOYSA-N

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象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Skin Sens. 1

储存分类代码

13 - Non Combustible Solids

WGK

WGK 2

闪点(°F)

150.1 °F

闪点(°C)

65.62 °C

个人防护装备

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

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Ariel Ceferino Toloza et al.
Memorias do Instituto Oswaldo Cruz, 101(1), 55-56 (2006-05-16)
New alternative insecticides are necessary for the chemical control of head lice. In this study the fumigant knockdown time 50% (KT50) and repellency index (RI) of three aliphatic lactones was compared with two essential oils and DDVP, against permethrin-resistance Pediculus
A R Dahl et al.
Biochemical pharmacology, 34(5), 631-636 (1985-03-01)
Eighteen methylenedioxyphenyl (MDP) compounds, including some commonly inhaled by people, were tested for the ability to inhibit rabbit nasal microsomal cytochrome P-450-dependent hexamethylphosphoramide (HMPA) N-demethylase. For comparison, liver microsomes were also used. Nasal cytochrome P-450 from rabbits metabolized MDP compounds
S Peock et al.
Journal of the Royal Society of Health, 113(6), 292-294 (1993-12-01)
Piperonal, once used to kill lice in Australian hospitals, was acclaimed as an effective pediculicide (Corlette, 1925) by the standards of the day. It is unusual in also exhibiting a repellent action against lice, a property only recently realised. A
The inhibition of rat nasal cytochrome P-450-dependent mono-oxygenase by the essence heliotropin (piperonal).
A R Dahl
Drug metabolism and disposition: the biological fate of chemicals, 10(5), 553-554 (1982-09-01)
S Yamauchi et al.
Bioscience, biotechnology, and biochemistry, 64(11), 2320-2327 (2001-02-24)
The threo-selective aldol condensation of (3R, 4S)-3-hydroxy-5-trityloxy-4-pentanolide, which was prepared from L-arabinose, with piperonal was applied to the stereoselective synthesis of the olivil type of lignan, (2R, 3R, 4R)-4-benzyl-4-hydroxy-3-hydroxymethyl-2-(3,4-methylenedioxyphenyl)tetrahydrofuran.

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Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.

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