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N-BOC-乙胺 | 38267-76-4

中文名称
N-BOC-乙胺
中文别名
——
英文名称
tert-butyl ethylcarbamate
英文别名
tert-butyl N-ethylcarbamate
N-BOC-乙胺化学式
CAS
38267-76-4
化学式
C7H15NO2
mdl
MFCD12923020
分子量
145.202
InChiKey
ISTGQSQWSKCNFJ-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    38-41℃
  • 溶解度:
    二氯甲烷、四氢呋喃

计算性质

  • 辛醇/水分配系数(LogP):
    1.3
  • 重原子数:
    10
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.857
  • 拓扑面积:
    38.3
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2924199090
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H315,H319,H335
  • 储存条件:
    存放在室温、干燥且密封的环境中。

SDS

SDS:201436101dfaa6edc13dd68e0f91f5c8
查看
Material Safety Data Sheet

Section 1. Identification of the substance
tert-Butyl N-ethylcarbamate
Product Name:
Synonyms:

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.
H315: Causes skin irritation
H319: Causes serious eye irritation
H335: May cause respiratory irritation
P261: Avoid breathing dust/fume/gas/mist/vapours/spray
Wear protective gloves/protective clothing/eye protection/face protection
P280:
P305+P351+P338: IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present
and easy to do – continue rinsing
P304+P340: IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing
P405: Store locked up

Section 3. Composition/information on ingredients.
tert-Butyl N-ethylcarbamate
Ingredient name:
CAS number: 38267-76-4

Section 4. First aid measures
Immediately wash skin with copious amounts of water for at least 15 minutes while removing
Skin contact:
contaminated clothing and shoes. If irritation persists, seek medical attention.
Eye contact: Immediately wash skin with copious amounts of water for at least 15 minutes. Assure adequate
flushing of the eyes by separating the eyelids with fingers. If irritation persists, seek medical
attention.
Inhalation: Remove to fresh air. In severe cases or if symptoms persist, seek medical attention.
Wash out mouth with copious amounts of water for at least 15 minutes. Seek medical attention.
Ingestion:

Section 5. Fire fighting measures
In the event of a fire involving this material, alone or in combination with other materials, use dry
powder or carbon dioxide extinguishers. Protective clothing and self-contained breathing apparatus
should be worn.

Section 6. Accidental release measures
Personal precautions: Wear suitable personal protective equipment which performs satisfactorily and meets local/state/national
standards.
Respiratory precaution: Wear approved mask/respirator
Hand precaution: Wear suitable gloves/gauntlets
Skin protection: Wear suitable protective clothing
Eye protection: Wear suitable eye protection
Methods for cleaning up: Mix with sand or similar inert absorbent material, sweep up and keep in a tightly closed container
for disposal. See section 12.
Environmental precautions: Do not allow material to enter drains or water courses.

Section 7. Handling and storage
Handling: This product should be handled only by, or under the close supervision of, those properly qualified
in the handling and use of potentially hazardous chemicals, who should take into account the fire,
health and chemical hazard data given on this sheet.
Storage: Store in closed vessels.

Section 8. Exposure Controls / Personal protection
Engineering Controls: Use only in a chemical fume hood.
Personal protective equipment: Wear laboratory clothing, chemical-resistant gloves and safety goggles.
General hydiene measures: Wash thoroughly after handling. Wash contaminated clothing before reuse.

Section 9. Physical and chemical properties
Not specified
Appearance:
Boiling point: No data
Melting point: No data
Flash point: No data
Density: No data
Molecular formula: C7H15NO2
Molecular weight: 145.2

Section 10. Stability and reactivity
Conditions to avoid: Heat, flames and sparks.
Materials to avoid: Oxidizing agents.
Possible hazardous combustion products: Carbon monoxide, nitrogen oxides.

Section 11. Toxicological information
No data.

Section 12. Ecological information
No data.

Section 13. Disposal consideration
Arrange disposal as special waste, by licensed disposal company, in consultation with local waste
disposal authority, in accordance with national and regional regulations.

Section 14. Transportation information
Non-harzardous for air and ground transportation.

Section 15. Regulatory information
No chemicals in this material are subject to the reporting requirements of SARA Title III, Section
302, or have known CAS numbers that exceed the threshold reporting levels established by SARA
Title III, Section 313.


SECTION 16 - ADDITIONAL INFORMATION
N/A

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    N-BOC-乙胺sodium periodateruthenium(IV) oxide hydrate 作用下, 以 乙酸乙酯 为溶剂, 反应 16.33h, 生成 乙酰基氨基甲酸叔丁酯
    参考文献:
    名称:
    氘修饰的碳青霉烯衍生物
    摘要:
    本发明属于医药技术领域,具体涉及氘修饰的碳青霉烯衍生物或其药用可接受的盐,制备这些化合物的方法,含有这些化合物的药物制剂和药物组合物,以及本发明氘修饰的碳青霉烯衍生物或其药用可接受的盐在制备用于治疗和/或预防感染性疾病的药物中的应用。
    公开号:
    CN112174965B
  • 作为产物:
    描述:
    tert-butyl (1-tosylethyl)carbamate 在 sodium tetrahydroborate 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 以77%的产率得到N-BOC-乙胺
    参考文献:
    名称:
    Reductive BOC-amination of aldehydes
    摘要:
    Base-assisted elimination-reduction of alpha -amidoalkyl sulfones with sodium borohydride proceeds in tetrahydrofuran at room temperature leading to the corresponding BOC-amines in good yields. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(01)00895-4
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文献信息

  • PHARMACEUTICAL COMPOUNDS AS INHIBITORS OF CELL PROLIFERATION AND THE USE THEREOF
    申请人:ANDERSON MARK B.
    公开号:US20100068197A1
    公开(公告)日:2010-03-18
    Disclosed are compounds of Formula I effective as cytotoxic agents. The compounds of this invention are useful in the treatment of a variety of clinical conditions in which uncontrolled growth and spread of abnormal cells occurs.
    揭示的是作为细胞毒性剂有效的I式化合物。本发明的化合物在治疗多种临床病况中是有用的,这些病况中发生异常细胞的不受控制的生长和扩散。
  • [EN] COMPOUNDS FOR THE TREATMENT OF HEPATITIS C<br/>[FR] COMPOSÉS DESTINÉS AU TRAITEMENT DE L'HÉPATITE C
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2012141704A1
    公开(公告)日:2012-10-18
    The disclosure provides compounds of formula I, including pharmaceutically acceptable salts, as well as compositions and methods of using the compounds. The compounds have activity against hepatitis C virus (HCV) and may be useful in treating those infected with HCV.
    该披露提供了公式I的化合物,包括药用可接受的盐,以及使用这些化合物的组合物和方法。这些化合物对丙型肝炎病毒(HCV)具有活性,并可能对感染HCV的人有用。
  • [EN] AMIDES AS PIM INHIBITORS<br/>[FR] AMIDES CONVENANT COMME INHIBITEURS DES PIM
    申请人:AMGEN INC
    公开号:WO2013130660A1
    公开(公告)日:2013-09-06
    The invention relates to amide-containing compounds of formula (1), and salts thereof. In some embodiments, the invention relates to inhibitors or modulators of Pim-1 and/or Pim-2, and/or Pim-3 protein kinase activity or enzyme function. In still further embodiments, the invention relates to pharmaceutical compositions comprising compounds disclosed herein, and their use in the prevention and treatment of Pim kinase related conditions and diseases, preferably cancer.
    本发明涉及式(1)的含酰胺化合物及其盐。在一些实施例中,本发明涉及Pim-1和/或Pim-2和/或Pim-3蛋白激酶活性或酶功能的抑制剂或调节剂。在更进一步的实施例中,本发明涉及包含本文披露的化合物的药物组合物,及其用于预防治疗Pim激酶相关状况和疾病,尤其是癌症的应用。
  • [EN] 6,7,8,9-TETRAHYDRO-5H-PYRIDO[2,3-d]AZEPINE DOPAMINE D3 LIGANDS<br/>[FR] LIGANDS 6,7,8,9-TÉTRAHYDRO-5H-PYRIDO[2,3-D]AZÉPINE DU RÉCEPTEUR D3 DE LA DOPAMINE
    申请人:PFIZER
    公开号:WO2017122116A1
    公开(公告)日:2017-07-20
    The present invention provides compounds of Formula (I): and pharmaceutically acceptable salts thereof wherein the variables R1, R2, R3, R4, R5, a and A are as defined herein; processes for the preparation of; intermediates used in the preparation of; and compositions containing such compounds or salts, and their uses for treating D3-mediated (or D3-associated) disorders including, e.g., substance addiction, substance abuse, schizophrenia (e.g., its cognitive symptoms), cognitive impairment (e.g., cognitive impairment associated with schizophrenia, AD or PD), Parkinson's disease, mania, anxiety, impulse control disorders, sexual disorders and depression.
    本发明提供了Formula (I)的化合物及其药学上可接受的盐,其中变量R1、R2、R3、R4、R5、a和A如本文所定义;制备方法;制备中使用的中间体;以及含有这种化合物或盐的组合物,以及它们用于治疗D3介导的(或与D3相关的)疾病,包括物质成瘾、物质滥用、精神分裂症(例如其认知症状)、认知障碍(例如与精神分裂症、阿尔茨海默病或帕森病相关的认知障碍)、帕森病、狂躁症、焦虑、冲动控制障碍、性功能障碍和抑郁症等疾病的用途。
  • [EN] COMPOUNDS AND USES THEREOF<br/>[FR] COMPOSÉS ET LEURS UTILISATIONS
    申请人:YUMANITY THERAPEUTICS INC
    公开号:WO2020198026A1
    公开(公告)日:2020-10-01
    The present invention features compounds useful in the treatment of neurological disorders and primary brain cancer. The compounds of the invention, alone or in combination with other pharmaceutically active agents, can be used for treating or preventing neurological disorders and primary brain cancer.
    本发明涉及对神经系统疾病和原发性脑癌治疗中有用的化合物。本发明的化合物,单独或与其他药用活性剂结合使用,可用于治疗或预防神经系统疾病和原发性脑癌。
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