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2-萘硼酸

2-萘硼酸用途

萘-2-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。

2-萘硼酸名称

[ CAS 号 ]:
32316-92-0

[ 中文名 ]:
2-萘硼酸

[ 英文名 ]:
2-Naphthaleneboronic acid

[中文别名 ]:

[英文别名 ]:

2-naphthaleneylboronic acid
2-naphthalene boronic acid
Naphthalene-2-boronic acid
Boronic acid, B-2-naphthalenyl-
naphthalen-2-ylboronic acid
2-Naphthaleneboronic acid
Naphthalenyl-2-boronic acid
2-Naphtahaleneboronic acid
Naphthalen-2-Yl-Boranediol
2-Naphthyl-phenylboronic acid

2-萘硼酸生物活性

[ 描述 ]:

萘-2-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

2-萘硼酸物理化学性质

[ 密度 ]:
1.2±0.1 g/cm3

[ 沸点 ]:
381.9±25.0 °C at 760 mmHg

[ 熔点 ]:
269-275 °C(lit.)

[ 分子式 ]:
C₁₀H₉BO₂

[ 分子量 ]:
171.99

[ 闪点 ]:
184.8±23.2 °C

[ 精确质量 ]:
172.069565

[ PSA ]:
40.46000

[ LogP ]:
2.82

[ 外观性状 ]:
黄色晶体粉末

[ 蒸汽压 ]:
0.0±0.9 mmHg at 25°C

[ 折射率 ]:
1.639

[ 储存条件 ]:
0-6°C

[ 水溶解性 ]:
水溶性：微溶；可溶于：甲醇

2-萘硼酸MSDS

2-萘硼酸安全信息

[ 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-S37/39

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

[ WGK德国 ]:
3

[ 海关编码 ]:
2931900090

2-萘硼酸合成路线

2-萘硼酸上下游产品

2-萘硼酸上游产品

2-萘硼酸下游产品

2-萘硼酸海关

[ 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%

2-萘硼酸文献

Novel styrylbenzene derivatives for detecting amyloid deposits.

Clin. Chim. Acta 436 , 27-34, (2014)

Various styrylbenzene compounds were synthesized and evaluated as mainly Aβ amyloid sensors. These compounds, however, cannot be used for detecting amyloid deposition in peripheral nerves because of t...

Enantioselective rhodium-catalyzed addition of arylboronic acids to trifluoromethyl ketones.

Chem. Commun. (Camb.) , 4093, (2006)

The catalytic asymmetric 1,2-addition of a series of arylboronic acids to 2,2,2-trifluoroacetophenones is described with high isolated yields (up to 96%) and good enantioselectivities (up to 83% ee) u...

Cationic palladium(II)-catalyzed addition of arylboronic acids to nitriles. One-step synthesis of benzofurans from phenoxyacetonitriles.

Org. Lett. 8 , 5987, (2006)

[Structure: see text] A cationic palladium complex catalyzed addition of arylboronic acids to nitriles to yield aryl ketones with moderate to good yields was developed. A one-step synthesis of benzofu...

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