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氮杂环丁烷盐酸盐

氮杂环丁烷盐酸盐用途

盐酸阿泽替丁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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氮杂环丁烷盐酸盐名称

[ CAS 号 ]:
36520-39-5

[ 中文名 ]:
氮杂环丁烷盐酸盐

[ 英文名 ]:
Azetidine hydrochloride

[中文别名 ]:

[英文别名 ]:

Azetidine, hydrochloride (1:1)
azetadine hydrochloride
Azetidinhydrochlorid
AZETIDINE HCL
azetidine monohydrochloride
Azacyclobutane Hydrochloride
Azetidine hydrochloride (1:1)
TRIMETHYLENEIMINE HYDROCHLORIDE
azetidinium chloride
hydrochloride salt of azetidine

氮杂环丁烷盐酸盐生物活性

[ 描述 ]:

盐酸阿泽替丁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

氮杂环丁烷盐酸盐物理化学性质

[ 沸点 ]:
103.8ºC at 760 mmHg

[ 熔点 ]:
>300 °C(lit.)

[ 分子式 ]:
C₃H₈ClN

[ 分子量 ]:
93.56

[ 闪点 ]:
152 °C

[ 精确质量 ]:
93.034531

[ PSA ]:
12.03000

[ LogP ]:
1.11050

[ 外观性状 ]:
白色粉末

[ 储存条件 ]:
Room temperature.

[ 水溶解性 ]:
水溶性：可溶

氮杂环丁烷盐酸盐MSDS

详细MSDS(安全技术说明书)

氮杂环丁烷盐酸盐安全信息

[ 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

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

[ WGK德国 ]:
3

[ 海关编码 ]:
2933990090

氮杂环丁烷盐酸盐海关

[ 海关编码 ]: 2933990090

[ 中文概述 ]:
2933990090. 其他仅含氮杂原子的杂环化合物. 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:20.0%

[ 申报要素 ]: 品名, 成分含量, 用途, 乌洛托品请注明外观, 6－己内酰胺请注明外观, 签约日期

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

氮杂环丁烷盐酸盐文献

Practical syntheses of N-substituted 3-hydroxyazetidines and 4-hydroxypiperidines by hydroxylation with Sphingomonas sp. HXN-200.

Org. Lett. 4 , 1859-1862, (2002)

[reaction: see text] Hydroxylation of N-substituted azetidines 11 and 12 and piperidines 15-19 with Sphingomonas sp. HXN-200 gave 91-98% of the corresponding 3-hydroxyazetidines 13 and 14 and 4-hydrox...

Domino formation of enamines--intramolecular cyclizations to 1-aminotetralins from γ-arylallene aldehydes and amines.

Org. Lett. 16(20) , 5438-41, (2014)

1,5-/1,6-Allenals conjugated to an aromatic ring undergo a cyclization, in the presence of an amine, that leads to tricyclic compounds including the 1-aminotetralin scaffold. This domino process combi...

Synthesis and biological evaluation of a novel phenyl substituted sydnone series as potential antitumor agents.

Bioorg. Med. Chem. Lett. 13 , 2899-2901, (2003)

A series of compounds containing an N-(4'-substituted-3'-nitrophenyl)sydnone moiety with potential antitumor activity was prepared based on active analogues. The rationale behind the design of these c...

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