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1H-苯并三唑-1-甲醇_分子结构_CAS_28539-02-8)
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1H-苯并三唑-1-甲醇

产品号 410233 公司名称 Sigma Aldrich
CAS号 28539-02-8 公司网站 http://www.sigmaaldrich.com
分子式 C7H7N3O 电 话 1-800-521-8956
分子量 149.14998 传 真
纯 度 98% 电子邮件
保 存 Chembase数据库ID: 87158

产品价格信息

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产品别名

标题
1H-Benzotriazole-1-methanol
IUPAC标准名
1H-1,2,3-benzotriazol-1-ylmethanol
IUPAC传统名
1,2,3-benzotriazol-1-ylmethanol
别名
1-(Hydroxymethyl)benzotriazole
1-Benzotriazolemethanol
NSC 12463

产品登记号

PubChem SID 24865702
MDL号 MFCD00179118
CAS号 28539-02-8

产品性质

Empirical Formula (Hill Notation) C7H7N3O
纯度 98%
熔点 150-152 °C(lit.)
GHS危险品标识 GHS07
GHS警示词 Warning
GHS危险声明 H315-H319-H335
欧盟危险性物质标志 刺激性(Irritant) 刺激性(Irritant) (Xi)
MSDS下载 下载链接
个人保护装置 dust mask type N95 (US), Eyeshields, Gloves
GHS警示性声明 P261-P305 + P351 + P338
危险公开号 36/37/38
安全公开号 26-36
德国WGK号 3

产品详细信息

详细说明 (English)
Application
Safe reagent for the in situ generation of anhydrous formaldehyde in organic solvents.8
Catalyst for:
• Hydrolysis of phenyl esters of a-furoic acid1Used as:
• Corrosion inhibitor of iron in aerated acidic media2
• Reactive oxygen scavenger3Reactant for:
• Synthesis of hydroxy-skipped bis-homo-inositols as potential glycosidase inhibitors via Sharpless asymmetric dihydroxylation and substrate-directed anionic hydroxymethylation4
• Enantioselective synthesis of aplysin utilizing a palladium-catalyzed addition of an arylboronic acid to an allenic alcohol, followed by Eschenmoser/Claisen rearrangement5
• Synthesis of substituted dihydroquinoline carboxylic acids as antitumor and HIV-1 integrase inhibitors6
• Gosteli-Claisen rearrangement7
Packaging
10, 50 g in glass bottle
详细说明 (简体中文)
Application
用于在有机溶剂中原位合成无水甲醛的安全剂。8
Catalyst for:
• Hydrolysis of phenyl esters of a-furoic acid1Used as:
• Corrosion inhibitor of iron in aerated acidic media2
• Reactive oxygen scavenger3Reactant for:
• Synthesis of hydroxy-skipped bis-homo-inositols as potential glycosidase inhibitors via Sharpless asymmetric dihydroxylation and substrate-directed anionic hydroxymethylation4
• Enantioselective synthesis of aplysin utilizing a palladium-catalyzed addition of an arylboronic acid to an allenic alcohol, followed by Eschenmoser/Claisen rearrangement5
• Synthesis of substituted dihydroquinoline carboxylic acids as antitumor and HIV-1 integrase inhibitors6
• Gosteli-Claisen rearrangement7
包装
10, 50 g in glass bottle

参考文献