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N-羟基-异丁酰胺 | 35613-84-4

中文名称
N-羟基-异丁酰胺
中文别名
N'-羟基-2-甲基法莫替丁;异丁脒肟
英文名称
isobutyramide oxime
英文别名
N'-hydroxyisobutyrimidamide;N-hydroxyisobutyramidine;N'-hydroxy-2-methylpropanimidamide;isobutyramidoxime
N-羟基-异丁酰胺化学式
CAS
35613-84-4
化学式
C4H10N2O
mdl
MFCD00464225
分子量
102.136
InChiKey
JHRDEHLFNLLCQS-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:
    60 °C
  • 沸点:
    146℃
  • 密度:
    1.09
  • 闪点:
    42℃
  • 溶解度:
    可溶于氯仿、甲醇
  • 稳定性/保质期:
    如果按照规格使用和储存,则不会分解,未有已知危险反应。

计算性质

  • 辛醇/水分配系数(LogP):
    0.4
  • 重原子数:
    7
  • 可旋转键数:
    1
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    58.6
  • 氢给体数:
    2
  • 氢受体数:
    2

安全信息

  • 危险等级:
    IRRITANT
  • 危险品标志:
    Xi
  • 安全说明:
    S45
  • 危险类别码:
    R25
  • 海关编码:
    2925290090
  • 包装等级:
    III
  • 危险类别:
    6.1
  • 危险性防范说明:
    P261,P264,P270,P271,P280,P301+P310,P302+P352,P304+P340,P305+P351+P338,P312,P330,P362,P403+P233,P405,P501
  • 危险品运输编号:
    2811
  • 危险性描述:
    H301,H315,H319,H335
  • 储存条件:
    请将贮藏器密封保存,并存放在阴凉干燥处。确保工作环境中具有良好的通风或排气设施。

SDS

SDS:6c24e0b39acc25a1465244327b99e03a
查看
Name: N -Hydroxy-2-methylpropanimidamide Material Safety Data Sheet
Synonym:
CAS: 35613-84-4
Section 1 - Chemical Product MSDS Name:N -Hydroxy-2-methylpropanimidamide Material Safety Data Sheet
Synonym:

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
35613-84-4 N'-Hydroxy-2-methylpropanimidamide 97+% unlisted
Hazard Symbols: XN
Risk Phrases: 20/21/22 36/37/38 44

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Harmful by inhalation, in contact with skin and if swallowed.
Irritating to eyes, respiratory system and skin. Risk of explosion if heated under confinement.
Potential Health Effects
Eye:
Causes eye irritation.
Skin:
Causes skin irritation. Harmful if absorbed through the skin.
Ingestion:
Harmful if swallowed. May cause irritation of the digestive tract.
Inhalation:
Harmful if inhaled. Causes respiratory tract irritation.
Chronic:
Not available.

Section 4 - FIRST AID MEASURES
Eyes: Flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Get medical aid.
Skin:
Get medical aid. Flush skin with plenty of water for at least 15 minutes while removing contaminated clothing and shoes.
Ingestion:
Get medical aid. Wash mouth out with water.
Inhalation:
Remove from exposure and move to fresh air immediately. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Get medical aid.
Notes to Physician:

Section 5 - FIRE FIGHTING MEASURES
General Information:
As in any fire, wear a self-contained breathing apparatus in pressure-demand, MSHA/NIOSH (approved or equivalent), and full protective gear. Violently decomposes when heated under confinement.
Risk of explosion if heated under confinement.
Extinguishing Media:
Use water spray, dry chemical, carbon dioxide, or chemical foam.

Section 6 - ACCIDENTAL RELEASE MEASURES
General Information: Use proper personal protective equipment as indicated in Section 8.
Spills/Leaks:
Vacuum or sweep up material and place into a suitable disposal container.

Section 7 - HANDLING and STORAGE
Handling:
Avoid breathing dust, vapor, mist, or gas. Avoid contact with skin and eyes.
Storage:
Store in a cool, dry place. Store in a tightly closed container.

Section 8 - EXPOSURE CONTROLS, PERSONAL PROTECTION
Engineering Controls:
Use adequate ventilation to keep airborne concentrations low.
Exposure Limits CAS# 35613-84-4: Personal Protective Equipment Eyes: Not available.
Skin:
Wear appropriate protective gloves to prevent skin exposure.
Clothing:
Wear appropriate protective clothing to prevent skin exposure.
Respirators:
Follow the OSHA respirator regulations found in 29 CFR 1910.134 or European Standard EN 149. Use a NIOSH/MSHA or European Standard EN 149 approved respirator if exposure limits are exceeded or if irritation or other symptoms are experienced.

Section 9 - PHYSICAL AND CHEMICAL PROPERTIES

Physical State: Solid
Color: White
Odor: Not available.
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: 60 - 61 deg C
Autoignition Temperature: Not available.
Flash Point: Not available.
Explosion Limits, lower: Not available.
Explosion Limits, upper: Not available.
Decomposition Temperature:
Solubility in water:
Specific Gravity/Density:
Molecular Formula: C4H10N2O
Molecular Weight: 102.14

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Stable under normal temperatures and pressures.
Conditions to Avoid:
High temperatures, incompatible materials.
Incompatibilities with Other Materials:
Strong oxidizing agents, reducing agents.
Hazardous Decomposition Products:
Carbon monoxide, oxides of nitrogen, carbon dioxide.
Hazardous Polymerization: Has not been reported

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 35613-84-4 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
N'-Hydroxy-2-methylpropanimidamide - Not listed by ACGIH, IARC, or NTP.

Section 12 - ECOLOGICAL INFORMATION


Section 13 - DISPOSAL CONSIDERATIONS
Dispose of in a manner consistent with federal, state, and local regulations.

Section 14 - TRANSPORT INFORMATION

IATA
Shipping Name: TOXIC SOLID, ORGANIC, N.O.S.*
Hazard Class: 6.1
UN Number: 2811
Packing Group: III
IMO
Shipping Name: TOXIC SOLID, ORGANIC, N.O.S.
Hazard Class: 6.1
UN Number: 2811
Packing Group: III
RID/ADR
Shipping Name: TOXIC SOLID, ORGANIC, N.O.S.
Hazard Class: 6.1
UN Number: 2811
Packing group: III

Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: XN
Risk Phrases:
R 20/21/22 Harmful by inhalation, in contact with
skin and if swallowed.
R 36/37/38 Irritating to eyes, respiratory system
and skin.
R 44 Risk of explosion if heated under confinement.
Safety Phrases:
S 15 Keep away from heat.
S 22 Do not breathe dust.
S 26 In case of contact with eyes, rinse immediately
with plenty of water and seek medical advice.
S 36/37/39 Wear suitable protective clothing, gloves
and eye/face protection.
WGK (Water Danger/Protection)
CAS# 35613-84-4: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 35613-84-4 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 35613-84-4 is not listed on the TSCA inventory.
It is for research and development use only.


SECTION 16 - ADDITIONAL INFORMATION
N/A

上下游信息

反应信息

  • 作为反应物:
    描述:
    N-羟基-异丁酰胺邻硝基苯磺酰氯N,N-二异丙基乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 24.0h, 以76%的产率得到isopropylcyanamide
    参考文献:
    名称:
    实用的合成氨酰胺肟的Tiemann重排的N-取代的氰胺。
    摘要:
    通过用苯磺酰氯(TsCl或邻-NsCl)和DIPEA进行mid胺肟的Tiemann重排,可以轻松而通用地合成各种N-取代的氰胺。
    DOI:
    10.1021/ol403645y
  • 作为产物:
    描述:
    异丁腈羟胺 作用下, 以 甲醇 为溶剂, 生成 N-羟基-异丁酰胺
    参考文献:
    名称:
    Dihydroxypyrimidine-4-carboxamides作为新型有效和选择性的HIV整合酶抑制剂。
    摘要:
    人类免疫缺陷病毒1型(HIV-1)整合酶是复制所需的三种组成型病毒酶之一,是化学疗法干预AIDS的合理靶标,最近在临床环境中也得到了证实。我们在这里报告的N-苄基5,6-二羟基嘧啶-4-羧酰胺的设计和合成作为一类药物,对HIV整合酶催化的链转移过程具有有效的抑制作用。在当前的研究中,对这些分子进行了结构修饰,以检查其对HIV整合酶抑制效能的影响。该系列中最有趣的化合物之一是2- [1-(二甲基氨基)-1-甲基乙基] -N-(4-氟苄基)-5,6-二羟基嘧啶-4-羧酰胺38,CIC95为78 nM。在血清蛋白存在下进行基于细胞的测定。
    DOI:
    10.1021/jm070027u
  • 作为试剂:
    描述:
    tert-butyl [6-(4-chlorophenyl)-1-methyl-4H-[1,2,4]triazolo[4,3-a][1]benzazepin-4-yl]acetate 、 sodium methylateN-羟基-异丁酰胺乙酸乙酯 、 Brine 、 Sodium sulfate-III 、 silica gel 、 methanol-dichloromethane 、 Isopropanol carbon dioxide 作用下, 以 N-甲基吡咯烷酮 为溶剂, 25.0~90.0 ℃ 、1999.83 MPa 条件下, 反应 13.0h, 以74 mg of the racemate were obtained的产率得到(-)-(4R)-6-(4-chlorophenyl)-1-methyl-4-{[3-(propan-2-yl)-1,2,4-oxadiazol-5-yl]methyl}-4H-[1,2,4]triazolo[4,3-a][1]benzazepine
    参考文献:
    名称:
    BET PROTEIN-INHIBITING 5-ARYL TRIAZOLE AZEPINES
    摘要:
    本发明涉及BET蛋白抑制剂,特别是通式(I)中的BRD4抑制剂5-芳基三唑氮杂环庚烷。其中R1,R2,R3和R4具有通式(I)所给出的含义,以及包含本发明化合物的制药组合物,以及其在高增殖性疾病,特别是恶性肿瘤疾病的预防和治疗中的预防和治疗用途。本发明还涉及在病毒感染,神经退行性疾病,炎症性疾病,动脉粥样硬化性疾病和男性生育控制中使用BET蛋白抑制剂。
    公开号:
    US20150299201A1
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文献信息

  • [EN] COMPOUNDS USEFUL AS CSF1 MODULATORS<br/>[FR] COMPOSÉS UTILES EN TANT QUE MODULATEURS DU FACTEUR 1 DE STIMULATION DE COLONIES
    申请人:REDX PHARMA PLC
    公开号:WO2016051193A1
    公开(公告)日:2016-04-07
    This invention relates to novel compounds and to pharmaceutical compositions comprising the novel compounds. More specifically, the invention relates to compounds useful as Colony Stimulating Factor 1 Receptor (cFMS) modulators (e.g. cFMS inhibitors). This invention also relates to processes for preparing the compounds, uses of the compounds in treatment and methods of treatment employing the compounds. Specifically, the invention relates to the use of the compounds for the treatment of cancer and autoimmune diseases.
    这项发明涉及新颖化合物以及包含这些新颖化合物的药物组合物。更具体地,该发明涉及用作集落刺激因子1受体(cFMS)调节剂(例如cFMS抑制剂)的化合物。这项发明还涉及制备这些化合物的方法,这些化合物在治疗中的用途以及利用这些化合物进行治疗的方法。具体而言,该发明涉及利用这些化合物治疗癌症和自身免疫性疾病。
  • THIAZOLYL-DIHYDRO-CHINAZOLINE
    申请人:Brandl Trixi
    公开号:US20070238746A1
    公开(公告)日:2007-10-11
    Disclosed are compounds of general formula (I), wherein the groups A, R 1 , R 2 , R a and R b have the meanings given in the claims and specification, the tautomers, racemates, enantiomers, diastereomers and the mixtures thereof, and optionally the pharmacologically acceptable acid addition salts, solvates and hydrates thereof, and processes for preparing these thiazolyl-dihydro-quinazolines and the use thereof as pharmaceutical compositions.
    揭示了一般式(I)的化合物, 其中,基团A,R1,R2,Ra和Rb具有权利要求和说明中给定的含义,其互变异构体,拉克酸盐,对映体,非对映体和它们的混合物,以及可选择的药理学上可接受的酸加盐,溶剂合物和水合物,以及制备这些噻唑基-二氢喹唑啉并将其用作药物组合物的方法。
  • THIAZOLYL-DIHYDRO-INDAZOLE
    申请人:Maier Udo
    公开号:US20070259855A1
    公开(公告)日:2007-11-08
    Disclosed are compounds of general formula (I), wherein the groups R 1 , R 2 , R a and R b have the meanings given in the claims and specification, the tautomers, racemates, enantiomers, diastereomers and the mixtures thereof, and optionally the pharmacologically acceptable acid addition salts, solvates and hydrates thereof, and processes for preparing these thiazolyl-dihydro-indazoles and the use thereof as pharmaceutical compositions.
    揭示了一般式(I)的化合物, 其中基团R1、R2、Ra和Rb具有权利要求和说明中给定的含义,其互变异构体、消旋体、对映体、非对映异构体及其混合物,以及可选择的药理学上可接受的酸加盐、溶剂化合物和水合物,以及制备这些噻唑基二氢吲唑烷并将其用作药物组合物的方法。
  • [EN] FUSED BICYCLIC PYRIMIDINE DERIVATIVES AND METHODS OF USE THEREOF<br/>[FR] DÉRIVÉS DE PYRIMIDINE BICYCLIQUES FUSIONNÉES ET LEURS PROCÉDÉS D'UTILISATION
    申请人:SCHERING CORP
    公开号:WO2011062885A1
    公开(公告)日:2011-05-26
    The present invention relates to Fused Bicyclic Pyrimidine Derivatives, compositions comprising a Fused Bicyclic Pyrimidine Derivative, and methods of using the Fused Bicyclic Pyrimidine Derivatives for treating or preventing obesity, diabetes, a metabolic disorder, a cardiovascular disease or a disorder related to the activity of a G-protein coupled receptor (GPCR) in a patient.
    本发明涉及融合双环嘧啶衍生物,包含融合双环嘧啶衍生物的组合物,以及利用融合双环嘧啶衍生物治疗或预防肥胖、糖尿病、代谢紊乱、心血管疾病或与患者体内G蛋白偶联受体(GPCR)活性相关的疾病的方法。
  • [EN] IMIDAZOPYRROLOPYRIDINE AS INHIBITORS OF THE JAK FAMILY OF KINASES<br/>[FR] IMIDAZOPYRROLOPYRIDINE EN TANT QU'INHIBITEURS DE LA FAMILLE JAK DE KINASES
    申请人:JANSSEN PHARMACEUTICA NV
    公开号:WO2018112382A1
    公开(公告)日:2018-06-21
    2-((1r,4r)-4-(imidazo[4,5-d]pyrrolo[2,3-b]pyridin-1(6H)-yl)cyclohexyl)acetonitrile compounds, pharmaceutical compositions containing them, methods of making them, and methods of using them including methods for treating disease states, disorders, and conditions mediated by JAK, such as inflammatory bowel disease.
    2-((1r,4r)-4-(imidazo[4,5-d]pyrrolo[2,3-b]pyridin-1(6H)-yl)cyclohexyl)acetonitrile化合物,含有它们的药物组合物,制备它们的方法,以及使用它们的方法,包括用于治疗由JAK介导的疾病状态、紊乱和疾病,如炎症性肠病的方法。
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