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(1S)-(+)-3-蒈烯

(1S)-(+)-3-蒈烯用途

【用途一】
用于有机溶剂和染料、医药及有机合成中间体

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(1S)-(+)-3-蒈烯名称

[ CAS 号 ]:
498-15-7

[ 中文名 ]:
(+)-3-蒈烯

[ 英文名 ]:
(+)-D-3-Carene

[中文别名 ]:

3-氯三氟甲苯

[英文别名 ]:

(1S)-(+)-3-Carene
Einecs 207-856-6
MFCD00066417

(1S)-(+)-3-蒈烯生物活性

[ 描述 ]:

(+)-3-苝烯是一种双环单萜烯,是松树精油的主要成分之一。(+)-3-苝烯是3-苝烯的(+)-对映体[1]。

[ 相关类别 ]:

信号通路 >> 其他 >> 其他

研究领域 >> 炎症/免疫

[参考文献]

[1]. Tsutomu. Sakai, et al. Volatile components of Douglas fir needles. J Agric Food Chem. 1967, 15, 6, 1070-1072.

(1S)-(+)-3-蒈烯物理化学性质

[ 密度 ]:
0.865

[ 沸点 ]:
170-172ºC

[ 分子式 ]:
C₁₀H₁₆

[ 分子量 ]:
136.23

[ 闪点 ]:
55ºC

[ 精确质量 ]:
136.12500

[ LogP ]:
2.99870

[ 蒸汽压 ]:
1.86mmHg at 25°C

[ 折射率 ]:
1.472

[ 储存条件 ]:
室温，干燥

(1S)-(+)-3-蒈烯MSDS

详细MSDS(安全技术说明书)

(1S)-(+)-3-蒈烯安全信息

[ 符号 ]:

GHS02, GHS07, GHS09

[ 信号词 ]:
Warning

[ 危害声明 ]:
H226-H317-H410

[ 警示性声明 ]:
P273-P280-P501

[ 个人防护装备 ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ 危害码 (欧洲) ]:
Xi:Irritant;N:Dangerousfortheenvironment;

[ 风险声明 (欧洲) ]:
R10;R50/53

[ 安全声明 (欧洲) ]:
S36/37-S60-S61

[ 危险品运输编码 ]:
UN 2319

[ WGK德国 ]:
2

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(1S)-(+)-3-蒈烯文献

Mechanisms for the formation of organic acids in the gas-phase ozonolysis of 3-carene.

Phys. Chem. Chem. Phys. 11(21) , 4184-97, (2009)

This paper describes experimental studies aimed at elucidating mechanisms for the formation of low-volatility organic acids in the gas-phase ozonolysis of 3-carene. Experiments were carried out in a s...

Antioxidant and antiacetylcholinesterase activities of some commercial essential oils and their major compounds.

Molecules 16(9) , 7672-90, (2011)

The commercial essential oils of Citrus aurantium L., Cupressus sempervirens L., Eucalyptus globulus Labill., Foeniculum vulgare Mill. and Thymus vulgaris L., isolated by steam distillation by a compa...

Asymmetric synthesis of α-methyl-α-amino acids via diastereoselective alkylation of (1S)-(+)-3-carene derived tricyclic iminolactone.

J. Org. Chem. 76(6) , 1621-33, (2011)

A novel carene-based alanine-equivalent tricyclic iminolactone 16 has been synthesized via stereoselective dihydroxylation of the double bond, IBX oxidation of the secondary alcohol, esterification of...

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