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甲基硼酸

甲基硼酸用途

甲基硼酸是一种生物化学试剂,可作为生物材料或有机化合物用于生命科学相关研究。

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甲基硼酸名称

[ CAS 号 ]:
13061-96-6

[ 中文名 ]:
甲基硼酸

[ 英文名 ]:
Methylboronic acid

[中文别名 ]:

[英文别名 ]:

methyl-boronic acid
Methylboronic acid
methaneboronic acid
UNII-8Z1ME41SCH
MFCD00002105
Boronic acid, B-methyl-
Dihydroxymethylborane
Methyl boronic acid

甲基硼酸生物活性

[ 描述 ]:

甲基硼酸是一种生物化学试剂,可作为生物材料或有机化合物用于生命科学相关研究。

[ 相关类别 ]:

研究领域 >> 其他

信号通路 >> 其他 >> 其他

甲基硼酸物理化学性质

[ 密度 ]:
1.0±0.1 g/cm3

[ 沸点 ]:
141.7±23.0 °C at 760 mmHg

[ 熔点 ]:
91-94 °C(lit.)

[ 分子式 ]:
CH₅BO₂

[ 分子量 ]:
59.86

[ 闪点 ]:
39.5±22.6 °C

[ 精确质量 ]:
60.038261

[ PSA ]:
40.46000

[ LogP ]:
-0.16

[ 外观性状 ]:
白色至淡黄色晶体粉末

[ 蒸汽压 ]:
2.4±0.6 mmHg at 25°C

[ 折射率 ]:
1.345

[ 储存条件 ]:
室温，密封

甲基硼酸MSDS

甲基硼酸安全信息

[ 符号 ]:

GHS07

[ 信号词 ]:
Warning

[ 危害声明 ]:
H315-H319-H335

[ 警示性声明 ]:
P261-P305 + P351 + P338

[ 个人防护装备 ]:
dust mask type N95 (US);Eyeshields;Gloves

[ 危害码 (欧洲) ]:
Xi:Irritant;

[ 风险声明 (欧洲) ]:
R36/37/38

[ 安全声明 (欧洲) ]:
S26-S36

[ 危险品运输编码 ]:
NONH for all modes of transport

[ WGK德国 ]:
3

[ 海关编码 ]:
2931900090

甲基硼酸合成路线

甲基硼酸上下游产品

甲基硼酸上游产品

甲基硼酸下游产品

甲基硼酸海关

[ 海关编码 ]: 2931900090

[ 中文概述 ]:
2931900090. 其他有机-无机化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:AB(入境货物通关单,出境货物通关单). 最惠国关税:6.5%. 普通关税:30.0%

[ Summary ]:
2931900090. other organo-inorganic compounds. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:6.5%. General tariff:30.0%

甲基硼酸文献

Effect of co-ligands on chemical and biological properties of (99m)Tc(III) complexes [(99m)Tc(L)(CDO)(CDOH)2BMe] (L=Cl, F, SCN and N3; CDOH2=cyclohexanedione dioxime).

Nucl. Med. Biol. 41(10) , 813-24, (2014)

(99m)Tc-Teboroxime ([(99m)TcCl(CDO)(CDOH)2BMe]) is a member of the BATO (boronic acid adducts of technetium dioximes) class of (99m)Tc(III) complexes. This study sought to explore the impact of co-lig...

Asymmetric bromolactonization using amino-thiocarbamate catalyst.

J. Am. Chem. Soc. 44th ed., 132 , 15474-15476, (2010)

A novel amino-thiocarbamate-catalyzed bromolactonization of unsaturated carboxylic acids has been developed. The scope of the reaction is evidenced by 22 examples of γ-lactones with up to 99% yield an...

Enantioselective bromoaminocyclization using amino-thiocarbamate catalysts.

J. Am. Chem. Soc. 133 , 9164-9167, (2011)

A facile and efficient enantioselective bromoaminocyclization of unsaturated sulfonamides has been developed using an amino-thiocarbamate catalyst. A range of enantioenriched pyrrolidines were prepare...

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