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N-叔丁氧羰基羟胺

N-叔丁氧羰基羟胺名称

[ CAS 号 ]:
36016-38-3

[ 中文名 ]:
N-羟基氨基甲酸叔丁酯

[ 英文名 ]:
tert-Butyl hydroxycarbamate

[中文别名 ]:

[英文别名 ]:

(tert-butyl)oxycarbohydroxamic acid
N-(tert-Butoxycarbonyl)hydroxylamine
tert-butyl N-hydroxy-carbamate
N-tert-Butoxycarbonylhydroxylamine
MFCD00002107
tert-Butyl hydroxycarbamate
t-Butyl N-hydroxycarbamate
EINECS 252-836-2
N-Boc-hydroxylamine
1,1-dimethylethyl N-hydroxycarbamate

N-叔丁氧羰基羟胺物理化学性质

[ 密度 ]:
1.1±0.1 g/cm3

[ 沸点 ]:
250.4±9.0 °C at 760 mmHg

[ 熔点 ]:
53-55 °C(lit.)

[ 分子式 ]:
C₅H₁₁NO₃

[ 分子量 ]:
133.146

[ 闪点 ]:
105.2±18.7 °C

[ 精确质量 ]:
133.073898

[ PSA ]:
58.56000

[ LogP ]:
0.82

[ 外观性状 ]:
潮湿的白色晶体

[ 蒸汽压 ]:
0.0±1.1 mmHg at 25°C

[ 折射率 ]:
1.443

[ 储存条件 ]:
2-8°C

N-叔丁氧羰基羟胺MSDS

详细MSDS(安全技术说明书)

N-叔丁氧羰基羟胺安全信息

[ 个人防护装备 ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ 危害码 (欧洲) ]:
Xi

[ 安全声明 (欧洲) ]:
S22-S24/25

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

[ WGK德国 ]:
3

[ 海关编码 ]:
29280090

N-叔丁氧羰基羟胺上下游产品

N-叔丁氧羰基羟胺上游产品

N-叔丁氧羰基羟胺下游产品

N-叔丁氧羰基羟胺海关

[ 海关编码 ]: 2924199090

[ 中文概述 ]:
2924199090. 其他无环酰胺（包括无环氨基甲酸酯)(包括其衍生物及盐）. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途, 包装

[ Summary ]:
2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

N-叔丁氧羰基羟胺文献

N-O chemistry for antibiotics: discovery of N-alkyl-N-(pyridin-2-yl)hydroxylamine scaffolds as selective antibacterial agents using nitroso Diels-Alder and ene chemistry.

J. Med. Chem. 54 , 6843-58, (2011)

The discovery, syntheses, and structure-activity relationships (SAR) of a new family of heterocyclic antibacterial compounds based on N-alkyl-N-(pyridin-2-yl)hydroxylamine scaffolds are described. A s...

Prodrugs of nitroxyl as inhibitors of aldehyde dehydrogenase.

J. Med. Chem. 35 , 3648, (1992)

In the preceding paper, analogs of chlorpropamide with an OMe substituent on the sulfonamide nitrogen were shown to inhibit aldehyde dehydrogenase (AlDH), and it was postulated that these compounds we...

Reactions of nitroso hetero-Diels-Alder cycloadducts with azides: stereoselective formation of triazolines and aziridines.

J. Org. Chem. 72 , 3929, (2007)

The addition of azides to acylnitroso hetero-Diels-Alder cycloadducts derived from cyclopentadiene affords exo-triazolines in excellent yield. The reaction is greatly affected by the level of alkene s...

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