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(S)-1-N-BOC-3-哌嗪甲酸甲酯 | 314741-39-4

中文名称
(S)-1-N-BOC-3-哌嗪甲酸甲酯
中文别名
(S)-1-N-叔丁氧羰基哌嗪-3-甲酸甲酯;S-1-BOC-3-哌嗪甲酸甲酯;(S)-N-4-Boc-2-哌嗪甲酸甲酯;(S)-1-N-Boc-3-哌嗪甲酸甲酯
英文名称
1-(tert-butyl) 3-methyl (S)-piperazine-1,3-dicarboxylate
英文别名
(S)-1-tert-butyl 3-methyl piperazine-1,3-dicarboxylate;methyl (S)‐1‐N‐boc‐piperazine‐3‐carboxylate;1-O-tert-butyl 3-O-methyl (3S)-piperazine-1,3-dicarboxylate
(S)-1-N-BOC-3-哌嗪甲酸甲酯化学式
CAS
314741-39-4
化学式
C11H20N2O4
mdl
——
分子量
244.291
InChiKey
QUKAHFCVKNRRBU-QMMMGPOBSA-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

  • 沸点:
    321.3±37.0 °C(Predicted)
  • 密度:
    1.118±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.4
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.82
  • 拓扑面积:
    67.9
  • 氢给体数:
    1
  • 氢受体数:
    5

安全信息

  • 海关编码:
    2933599090
  • 危险性防范说明:
    P261,P280,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H332,H335
  • 储存条件:
    2-8°C

SDS

SDS:37b639a1876833b9f6ea205d89da6fcd
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: Methyl (S)-4-Boc-piperazine-2-carboxylate
Synonyms: 1-tert-Butyl 3-methyl (3S)-piperazine-1,3-dicarboxylate

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.

Section 3. Composition/information on ingredients.
Ingredient name: Methyl (S)-4-Boc-piperazine-2-carboxylate
CAS number: 314741-39-4

Section 4. First aid measures
Skin contact: Immediately wash skin with copious amounts of water for at least 15 minutes while removing
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.
Ingestion: Wash out mouth with copious amounts of water for at least 15 minutes. Seek medical attention.

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.
Store in closed vessels, refrigerated.
Storage:

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
Appearance: Not specified
Boiling point: No data
No data
Melting point:
Flash point: No data
Density: No data
Molecular formula: C11H20N2O4
Molecular weight: 244.3

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:
    (S)-1-N-BOC-3-哌嗪甲酸甲酯盐酸 作用下, 以 甲醇 为溶剂, 反应 1.0h, 生成 (S)-methyl piperazine-2-carboxylate hydrochloride
    参考文献:
    名称:
    [EN] COMBINATION THERAPIES FOR TREATMENT OF CANCER
    [FR] THÉRAPIES COMBINATOIRES POUR LE TRAITEMENT DU CANCER
    摘要:
    提供用于治疗与KRAS基因突变相关的癌症的联合疗法。还提供了包含治疗剂的组合物,用于治疗与KRAS基因突变相关的癌症。
    公开号:
    WO2016044772A1
  • 作为产物:
    参考文献:
    名称:
    Compounds and methods for the treatment of neoplastic disease
    摘要:
    一种调节异常细胞拓扑异构酶酶活性的方法,涉及将该酶与抑制其介导的与酶形成复合物的多核苷酸底物的剪切的化合物接触。含有这种化合物的制药组合物可用于治疗肿瘤或抑制某些癌细胞的生长。筛选方法可用于识别其他用于这些用途的化合物。
    公开号:
    US20030203917A1
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文献信息

  • [EN] INHIBITORS OF KRAS G12C<br/>[FR] INHIBITEURS DE K-RAS G12C
    申请人:ARAXES PHARMA LLC
    公开号:WO2015054572A1
    公开(公告)日:2015-04-16
    Compounds having activity as inhibitors of G12C mutant KRAS protein are provided. The compounds have the following structure (I): or a pharmaceutically acceptable salt, tautomer, prodrug or stereoisomer thereof, wherein R1, R2a, R3a, R3b, R4a, R4b, G1, G2, L1, L2, m1, m2, A, B, W, X, Y, Z and E are as defined herein. Methods associated with preparation and use of such compounds, pharmaceutical compositions comprising such compounds and methods to modulate the activity of G12C mutant KRAS protein for treatment of disorders, such as cancer, are also provided.
    提供了作为G12C突变KRAS蛋白抑制剂活性的化合物。这些化合物具有以下结构(I):或其药用可接受的盐、互变异构体、前药或立体异构体,其中R1、R2a、R3a、R3b、R4a、R4b、G1、G2、L1、L2、m1、m2、A、B、W、X、Y、Z和E如本文所定义。还提供了与制备和使用这些化合物相关的方法,包括含有这些化合物的药物组合物以及调节G12C突变KRAS蛋白活性以治疗癌症等疾病的方法。
  • [EN] CYANO-SUBSTITUTED HETEROCYCLES WITH ACTIVITY AS INHIBITORS OF USP30<br/>[FR] HÉTÉROCYCLES CYANO-SUBSTITUÉS PRÉSENTANT UNE ACTIVITÉ EN TANT QU'INHIBITEURS DE L'USP30
    申请人:MISSION THERAPEUTICS LTD
    公开号:WO2018065768A1
    公开(公告)日:2018-04-12
    The present invention relates to cyano-substituted-heterocycles of Formula (I) with activity as inhibitors of deubiquitilating enzymes, in particular, ubiquitin C-terminal hydrolase 30 or ubiquitin specific peptidase 30 (USP30), having utility in a variety of therapeutic areas including cancer and conditions involving mitochondrial dysfunction. (Formula (I))
    本发明涉及具有抑制去泛素化酶活性的Formula (I)的氰基取代杂环化合物,特别是泛素C-末端水解酶30或泛素特异性肽酶30(USP30),在包括癌症和涉及线粒体功能障碍等各种治疗领域中具有用途。(Formula (I))
  • PHENYL AMINO PIPERIDINE mTORC INHIBITORS AND USES THEREOF
    申请人:Navitor Pharmaceuticals, Inc.
    公开号:US20180127370A1
    公开(公告)日:2018-05-10
    The present invention provides compounds, compositions thereof, and methods of using the same.
    本发明提供了化合物、其组合物以及使用它们的方法。
  • Furo-3-carboxamide derivatives and methods of use
    申请人:AbbVie Inc.
    公开号:US09777020B2
    公开(公告)日:2017-10-03
    Compounds of formula (I) and pharmaceutically acceptable salts, esters, amides, or radiolabelled forms thereof, wherein R1, Z1, Z2, and n are as defined in the specification, are useful in treating conditions or disorders prevented by or ameliorated by Tropomysin receptor kinases (Trk). Methods for making the compounds are disclosed. Also disclosed are pharmaceutical compositions of compounds of formula (I), and methods for using such compounds and compositions.
    式(I)的化合物及其药学上可接受的盐、酯、酰胺或放射标记形式,在该式中R1、Z1、Z2和n如规范中所定义,可用于治疗由Tropomysin受体激酶(Trk)预防或改善的症状或疾病。公开了制备这些化合物的方法。还公开了式(I)化合物的药物组合物,以及使用这些化合物和组合物的方法。
  • [EN] FACTOR XIIa INHIBITORS<br/>[FR] INHIBITEURS DU FACTEUR XIIA
    申请人:MERCK SHARP & DOHME
    公开号:WO2018093695A1
    公开(公告)日:2018-05-24
    The present invention provides a compound of Formula (I) and pharmaceutical compositions comprising one or more said compounds, and methods for using said compounds for treating or preventing thromboses, embolisms, hypercoagulability or fibrotic changes. The compounds are selective Factor XIIa inhibitors.
    本发明提供了一种化合物(I)及包含一种或多种所述化合物的药物组合物,以及使用所述化合物治疗或预防血栓、栓塞、高凝状态或纤维化变化的方法。这些化合物是选择性凝血因子XIIa抑制剂。
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