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甲酰乙内脲 | 616-04-6

中文名称
甲酰乙内脲
中文别名
1-甲基乙内酰脲;1-甲基海因
英文名称
1-methyldiazolidine-2,4-dione
英文别名
1-methylhydantoin;1-methylimidazolidine-2,4-dione
甲酰乙内脲化学式
CAS
616-04-6
化学式
C4H6N2O2
mdl
MFCD00003187
分子量
114.104
InChiKey
RHYBFKMFHLPQPH-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:
    156-157 °C(lit.)
  • 沸点:
    213.59°C (rough estimate)
  • 密度:
    1.284
  • 溶解度:
    可溶于DMSO(少许)、甲醇(少许)
  • 物理描述:
    Solid
  • 稳定性/保质期:

    性质与稳定性:在常温常压下,该物质不会分解。

计算性质

  • 辛醇/水分配系数(LogP):
    -0.9
  • 重原子数:
    8
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    49.4
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 危险品标志:
    Xi
  • 安全说明:
    S24/25
  • WGK Germany:
    3
  • 海关编码:
    2933990090
  • 危险性防范说明:
    P261,P301+P312,P302+P352,P304+P340,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335
  • 储存条件:
    贮存:将密器密封后,储存在密封的主要容器中,并置于阴凉、干燥处。

SDS

SDS:64cd163d03f01cb4773e01912c98a632
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Name: 1-Methylhydantoin 97% Material Safety Data Sheet
Synonym: None
CAS: 616-04-6
Section 1 - Chemical Product MSDS Name:1-Methylhydantoin 97% Material Safety Data Sheet
Synonym:None

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
616-04-6 1-methylhydantoin 97.0 210-460-6
Hazard Symbols: None Listed.
Risk Phrases: None Listed.

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
The toxicological properties of this material have not been fully investigated.
Potential Health Effects
Eye:
May cause eye irritation.
Skin:
May cause skin irritation.
Ingestion:
May cause irritation of the digestive tract. The toxicological properties of this substance have not been fully investigated.
Inhalation:
May cause respiratory tract irritation. The toxicological properties of this substance have not been fully investigated.
Chronic:
No information found.

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 immediately.
Skin:
Get medical aid. Flush skin with plenty of water for at least 15 minutes while removing contaminated clothing and shoes. Wash clothing before reuse.
Ingestion:
If victim is conscious and alert, give 2-4 cupfuls of milk or water.
Never give anything by mouth to an unconscious person. Get medical aid immediately.
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:
Antidote: None reported.

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. During a fire, irritating and highly toxic gases may be generated by thermal decomposition or combustion.
Extinguishing Media:
Use water spray, dry chemical, carbon dioxide, or appropriate foam.

Section 6 - ACCIDENTAL RELEASE MEASURES
General Information: Use proper personal protective equipment as indicated in Section 8.
Spills/Leaks:
Clean up spills immediately, observing precautions in the Protective Equipment section. Sweep up or absorb material, then place into a suitable clean, dry, closed container for disposal. Avoid generating dusty conditions. Provide ventilation.

Section 7 - HANDLING and STORAGE
Handling:
Wash thoroughly after handling. Remove contaminated clothing and wash before reuse. Use with adequate ventilation. Minimize dust generation and accumulation. Avoid contact with eyes, skin, and clothing. Keep container tightly closed. Avoid ingestion and inhalation.
Storage:
Keep container closed when not in use. Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.

Section 8 - EXPOSURE CONTROLS, PERSONAL PROTECTION
Engineering Controls:
Use adequate ventilation to keep airborne concentrations low.
Exposure Limits CAS# 616-04-6: Personal Protective Equipment Eyes: Wear appropriate protective eyeglasses or chemical safety goggles as described by OSHA's eye and face protection regulations in 29 CFR 1910.133 or European Standard EN166.
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: 156.00 - 157.00 deg C
Autoignition Temperature: Not available.
Flash Point: Not available.
Explosion Limits, lower: N/A
Explosion Limits, upper: N/A
Decomposition Temperature:
Solubility in water:
Specific Gravity/Density:
Molecular Formula: C4H6N2O2
Molecular Weight: 114.10

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Stable under normal temperatures and pressures.
Conditions to Avoid:
Incompatible materials, dust generation, strong oxidants.
Incompatibilities with Other Materials:
Strong oxidizing agents.
Hazardous Decomposition Products:
Carbon monoxide, oxides of nitrogen, irritating and toxic fumes and gases, carbon dioxide.
Hazardous Polymerization: Has not been reported

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 616-04-6 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
1-methylhydantoin - Not listed by ACGIH, IARC, or NTP.

Section 12 - ECOLOGICAL INFORMATION
Other No information available.

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

Section 14 - TRANSPORT INFORMATION

IATA
Not regulated as a hazardous material.
IMO
Not regulated as a hazardous material.
RID/ADR
Not regulated as a hazardous material.

Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: Not available.
Risk Phrases:
Safety Phrases:
S 24/25 Avoid contact with skin and eyes.
S 28A After contact with skin, wash immediately with
plenty of water.
S 37 Wear suitable gloves.
S 45 In case of accident or if you feel unwell, seek
medical advice immediately (show the label where
possible).
WGK (Water Danger/Protection)
CAS# 616-04-6: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 616-04-6 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 616-04-6 is not listed on the TSCA inventory.
It is for research and development use only.


SECTION 16 - ADDITIONAL INFORMATION
N/A

制备方法与用途

生物活性

N-甲基异(1-甲基异、二氧肌酐)是一种小分子极性底物,是肌酸酐经细菌降解后的产物。

靶点

人类内源代谢物

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:
    甲酰乙内脲 作用下, 以 溶剂黄146 为溶剂, 生成 5-溴-1-甲基咪唑烷-2,4-二酮
    参考文献:
    名称:
    Compounds for treating tumors
    摘要:
    该发明提供了以下式(I)的化合物: 其中E、A、B′、R6、R7、R8和R9在规范中定义,这些化合物表现出抗癌活性,并可用于治疗癌症。
    公开号:
    US20050037977A1
  • 作为产物:
    描述:
    肌酸barium dihydroxide 作用下, 生成 甲酰乙内脲
    参考文献:
    名称:
    Neubauer, Justus Liebigs Annalen der Chemie, 1866, vol. 137, p. 294
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • DIARYLMETHYLAMIDE DERIVATIVE HAVING ANTAGONISTIC ACTIVITY ON MELANIN-CONCENTRATING HORMONE RECEPTOR
    申请人:Banyu Pharmaceutical Co., Ltd.
    公开号:EP2272841A1
    公开(公告)日:2011-01-12
    [Problem] To provide a melanin-concentrating hormone receptor antagonist useful as a pharmaceutical agent for central diseases, circulatory diseases, and metabolic diseases. [Means for Resolution] Provided is a diarylmethylamide derivative represented by formula (I): Wherein R1a, R1b, R2a, R2b, R3a, and R3b independently represent a hydrogen atom or the like, R4 represents a hydrogen atom, C1-6 alkyl, or the like, R5 represents a hydrogen atom or the like, Z represents C1-6 alkyl or the like, or R4 and Z together form a 4- to 6-membered nitrogen-containing hetero ring, Y1 represents H or the like, Y2 represents H, or Y1 and Y2 together form - O-CH2-, W represents C, SO, or the like, Ar1 represents 6-membered aryl or the like, Ar2 represents 6-membered aryl or the like, and ring A represents a benzene ring, a pyridine ring, or the like.
    [问题] 提供一种对黑色素浓缩激素受体拮抗剂,用作中枢疾病、循环疾病和代谢疾病的药用制剂。 [解决方法] 提供一种由式(I)表示的二芳基甲酰胺衍生物: 其中R1a、R1b、R2a、R2b、R3a和R3b独立地表示氢原子或类似物,R4表示氢原子、C1-6烷基或类似物,R5表示氢原子或类似物,Z表示C1-6烷基或类似物,或者R4和Z一起形成一个含氮杂环的4-至6-成员环,Y1表示H或类似物,Y2表示H,或者Y1和Y2一起形成-O-CH2-,W表示C、SO或类似物,Ar1表示6-成员芳基或类似物,Ar2表示6-成员芳基或类似物,环A表示苯环、吡啶环或类似物。
  • Development of New Hydroxamate Matrix Metalloproteinase Inhibitors Derived from Functionalized 4-Aminoprolines
    作者:Michael G. Natchus、Roger G. Bookland、Biswanath De、Neil G. Almstead、Stanislaw Pikul、Michael J. Janusz、Sandra A. Heitmeyer、Erin B. Hookfin、Lily C. Hsieh、Martin E. Dowty、Charles R. Dietsch、Vikram S. Patel、Susan M. Garver、Fei Gu、Matthew E. Pokross、Glen E. Mieling、Timothy R. Baker、David J. Foltz、Sean X. Peng、David M. Bornes、Michael J. Strojnowski、Yetunde O. Taiwo
    DOI:10.1021/jm000246e
    日期:2000.12.1
    activity with sub-nanomolar potency for some enzymes. Modifications of the P1' portion of the molecule played a key role in affecting both potency and selectivity within the MMP family. Longer-chain aliphatic substituents in this region of the molecule tended to increase potency for MMP-3 and decrease potency for MMP-1, as exemplified by compounds 48-50, while aromatic substituents, as in compound 52, generated
    基脯酸支架制备了一系列异羟酸酯,并测试了其作为基质蛋白酶(MMP)抑制剂的功效。据报道该系列的详细SAR是针对MMP家族中的5种酶,许多抑制剂(例如化合物47)具有广谱活性,某些酶具有亚纳摩尔的效力。分子P1'部分的修饰在影响MMP家族内的效能和选择性方面起着关键作用。如化合物48-50所示,在分子的该区域中的长链脂族取代基倾向于增加对MMP-3的效力而降低对MMP-1的效力,而如化合物52中的芳族取代基产生广谱抑制作用。该数据基于X射线晶体数据也被合理化。虽然体外经口吸收似乎不太可预测,但随着更长和更多亲性取代基的出现,吸收率往往会降低。最后,使用骨关节炎的大鼠模型评估这些化合物的功效,并在它们的药代动力学和体内功效之间建立了直接联系。
  • [EN] PROCESS FOR THE PREPARATION OF HERBICIDAL COMPOUNDS<br/>[FR] PROCÉDÉ DE PRÉPARATION DE COMPOSÉS HERBICIDES
    申请人:SYNGENTA PARTICIPATIONS AG
    公开号:WO2017186621A1
    公开(公告)日:2017-11-02
    The present invention relates to a process for the preparation of a compound of formula (IX) wherein R1, R2A, R2B, R3, R4, R5 and R6 are as defined in the specification. Furthermore, the present invention also relates to reduction of the compound of formula (IX) to produce a compound of formula (I).
    本发明涉及一种制备式(IX)化合物的方法,其中R1、R2A、R2B、R3、R4、R5和R6如规范中所定义。此外,本发明还涉及将式(IX)化合物还原以产生式(I)化合物的方法。
  • PYRIDIN-2-ONE DERIVATIVES OF FORMULA (I) USEFUL AS EP3 RECEPTOR ANTAGONISTS
    申请人:Janssen Pharmaceutica NV
    公开号:US20190047959A1
    公开(公告)日:2019-02-14
    The present invention is directed to pyridin-2-one derivatives, pharmaceutical compositions containing them and their use as antagonists of the EP3 receptor, for the treatment of for example, impaired oral glucose tolerance, elevated fasting glucose, Type II Diabetes Mellitus, Syndrome X (also known as Metabolic Syndrome) and related disorders and complications thereof.
    本发明涉及吡啶-2-酮衍生物,包含它们的药物组合物以及它们作为EP3受体的拮抗剂的使用,用于治疗例如受损的口服葡萄糖耐量、空腹血糖升高、2型糖尿病、综合征X(也称为代谢综合征)及其相关疾病和并发症。
  • PYRIDIN-2-ONE DERIVATIVES OF FORMULA (III) USEFUL AS EP3 RECEPTOR ANTAGONISTS
    申请人:Janssen Pharmaceutica NV
    公开号:US20190047961A1
    公开(公告)日:2019-02-14
    The present invention is directed to pyridin-2-one derivatives, pharmaceutical compositions containing them and their use as antagonists of the EP3 receptor, for the treatment of for example, impaired oral glucose tolerance, elevated fasting glucose, Type II Diabetes Mellitus, Syndrome X (also known as Metabolic Syndrome) and related disorders and complications thereof.
    本发明涉及吡啶-2-酮衍生物,包含它们的药物组合物以及它们作为EP3受体的拮抗剂的使用,用于治疗例如受损的口服葡萄糖耐量,空腹血糖升高,2型糖尿病,综合征X(也称为代谢综合征)以及与之相关的疾病和并发症。
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
hnmr
mass
cnmr
ir
raman
  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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同类化合物

(4S,4''S)-2,2''-环亚丙基双[4-叔丁基-4,5-二氢恶唑] 香豆素-6-羧酸 顺式-3a,5,6,6a-四氢-3-(1-甲基乙基)-4H-环戊二烯并[d]异恶唑 锌离子载体IV 钐(III) 离子载体 II 苯,1-(2E)-2-丁烯-1-基-2-氟- 苯,(2,2-二氟乙烯基)- 聚二硫二噻唑烷 缩胆囊肽9 绕丹酸钠 盐(1:?)5'-尿苷酸,钠 甲酰乙内脲 甲巯咪唑 甲基羟甲基油基噁唑啉 甲基5-羟基-3,5-二甲基-4,5-二氢-1H-吡唑-1-羧酸酯 甲基5-甲基-4,5-二氢-1H-吡唑-3-羧酸酯 甲基5-甲基-4,5-二氢-1H-吡唑-1-羧酸酯 甲基5-氰基-4,5-二氢-1,2-恶唑-3-羧酸酯 甲基5-乙炔基-4,5-二氢-1H-吡唑-3-羧酸酯 甲基5-(羟基甲基)-4,5-二氢-1,2-恶唑-3-羧酸酯 甲基4-甲基-5-氧代-4,5-二氢-1H-吡唑-3-羧酸酯 甲基4-甲基-4,5-二氢-1H-吡唑-3-羧酸酯 甲基4-乙炔基-4,5-二氢-1H-吡唑-3-羧酸酯 甲基4,5-二氮杂螺[2.4]庚-5-烯-6-羧酸酯 甲基4,5-二氢-5-乙基-1H-吡唑-1-羧酸酯 甲基3-甲基-4,5-二氢-1,2-恶唑-4-羧酸酯 甲基(E)-3-[6-[1-羟基-1-(4-甲基苯基)-3-(1-吡咯烷基)丙基]-2-吡啶基]丙烯酰酸酯 甲基(5-氧代-4,5-二氢-1,2-恶唑-3-基)乙酸酯 环戊二烯并[d]咪唑-2,5(1H,3H)-二硫酮 环己羧酸,3-氨基-2-甲氧基-,甲基酯,(1S,2S,3S)- 溶剂黄93 溴化1-十六烷基-3-甲基咪唑 溴化1-十二烷基-2,3-二甲基咪唑 泰比培南酯中间体 泰比培南酯中间体 氨甲酸,[4,5-二氢-4-(碘甲基)-2-噻唑基]-,1,1-二甲基乙基酯(9CI) 氨基甲硫酸,[2-[[(2-羰基-1-咪唑烷基)硫代甲基]氨基]乙基]-,O-甲基酯 异噻唑,4,5-二氯-2,5-二氢-2-辛基- 希诺米啉 四氟硼酸二氢1,3-二(叔-丁基)-4,5--1H-咪唑正离子 四唑硝基紫 噻唑烷-2,4-二酮-2-缩氨基脲 噻唑丁炎酮 噻唑,4,5-二氢-4-(1-甲基乙基)-,(S)- 噁唑,4,5-二氢-4,4-二甲基-2-(5-甲基-2-呋喃基)- 噁唑,2-庚基-4,5-二氢- 咪唑烷基脲 吡嗪,2,3-二氢-5,6-二甲基-2-丙基- 叔-丁基3-羟基-1,4,6,7-四氢吡唑并[4,3-c]吡啶-5-羧酸酯 双吡唑啉酮