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5-溴-2-氯-n-甲基苯甲酰胺 | 435273-54-4

中文名称
5-溴-2-氯-n-甲基苯甲酰胺
中文别名
——
英文名称
5-bromo-2-chloro-N-methylbenzamide
英文别名
N-methyl-6-chloro-3-bromobenzamide
5-溴-2-氯-n-甲基苯甲酰胺化学式
CAS
435273-54-4
化学式
C8H7BrClNO
mdl
MFCD05853706
分子量
248.507
InChiKey
JKYTZJSGPWNIRB-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

计算性质

  • 辛醇/水分配系数(LogP):
    2.6
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.125
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 氢受体数:
    1

安全信息

  • 危险等级:
    IRRITANT
  • 海关编码:
    2924299090

SDS

SDS:9663930596e3c940554b0b6f292bac02
查看
Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: Methyl 5-bromo-2-chlorobenzamide
Synonyms: 5-Bromo-2-chloro-N-methylbenzamide

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

Section 3. Composition/information on ingredients.
Ingredient name: Methyl 5-bromo-2-chlorobenzamide
CAS number: 435273-54-4

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.
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: C8H7BrClNO
Molecular weight: 248.5

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, hydrogen chloride, hydrogen bromide.

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

反应信息

  • 作为反应物:
    描述:
    5-溴-2-氯-n-甲基苯甲酰胺potassium phosphate四(三苯基膦)钯1,1'-双(二苯膦基)二茂铁二氯化钯(II)二氯甲烷复合物potassium acetate 作用下, 以 1,4-二氧六环 为溶剂, 反应 12.0h, 生成 ethyl 4-{7-amino-3-[4-chloro-3-(methylcarbamoyl)phenyl]-2-methylpyrazolo[1,5-a]-pyrimidin-5-yl}piperazine-1-carboxylate
    参考文献:
    名称:
    [EN] FUSED PYRAZOLE DERIVATIVES AS KINASE INHIBITORS
    [FR] DÉRIVÉS DE PYRAZOLE CONDENSÉS EN TANT QU'INHIBITEURS DE KINASE
    摘要:
    一系列经替代的嘧唑并[1,5-a]嘧啶和嘧唑并[1,5-a][1,3,5]-三嗪衍生物,其化学式定义如下,作为选择性抑制磷脂酰肌醇-4-激酶ΙΙΙβ(ΡI4ΚΙΙΙβ)活性的药物,在治疗和/或预防各种人类疾病方面具有益处,包括炎症性、自身免疫性和肿瘤性疾病;病毒性疾病和疟疾;以及器官和细胞移植排斥。
    公开号:
    WO2017055305A1
  • 作为产物:
    描述:
    5-溴-2-氯苯甲酸甲胺草酰氯N,N-二甲基甲酰胺N,N-二异丙基乙胺 作用下, 以 二氯甲烷四氢呋喃 为溶剂, 反应 2.33h, 以100%的产率得到5-溴-2-氯-n-甲基苯甲酰胺
    参考文献:
    名称:
    [EN] FUSED PYRAZOLE DERIVATIVES AS KINASE INHIBITORS
    [FR] DÉRIVÉS DE PYRAZOLE CONDENSÉS EN TANT QU'INHIBITEURS DE KINASE
    摘要:
    一系列经替代的嘧唑并[1,5-a]嘧啶和嘧唑并[1,5-a][1,3,5]-三嗪衍生物,其化学式定义如下,作为选择性抑制磷脂酰肌醇-4-激酶ΙΙΙβ(ΡI4ΚΙΙΙβ)活性的药物,在治疗和/或预防各种人类疾病方面具有益处,包括炎症性、自身免疫性和肿瘤性疾病;病毒性疾病和疟疾;以及器官和细胞移植排斥。
    公开号:
    WO2017055305A1
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文献信息

  • [EN] BIPHENYL DERIVATIVE OR ITS SALT, AND PESTICIDE CONTAINING IT AS AN ACTIVE INGREDIENT<br/>[FR] DERIVE DE DIPHENYLE OU SES SELS, ET PESTICIDE DONT IL CONSTITUE LE PRINCIPE ACTIF
    申请人:ISHIHARA SANGYO KAISHA
    公开号:WO2005044007A1
    公开(公告)日:2005-05-19
    A pesticide having stabilized high pesticidal effects for crop plants infected with plant diseases, is presented. The pesticide contains a biphenyl derivative represented by the formula (I) or its salt, as an active ingredient: wherein X, Y and Z are each independently a halogen atom, a hydroxyl group, a formyl group, an alkyl group which may be substituted, an alkoxy group which may be substituted, an alkylthio group, an alkylsulfonyl group, an alkylsulfinyl group, or the like, A is a carbonyl group, a thiocarbonyl group, an alkylene group, or a single bond, R1 and R2 are each independently a hydrogen atom, an alkyl group which may be substituted, an alkenyl group which may be substituted, an alkynyl group which may be substituted, an aryl group which may be substituted, a formyl group, an alkylcarbonyl group, a cyano group, or the like, and m and n are each independently 0, 1, 2, 3 or 4.
    一种对感染植物病害的作物植物具有稳定高效杀虫效果的杀虫剂被提出。该杀虫剂含有作为活性成分的二苯基衍生物,该衍生物由公式(I)表示或其盐类:其中X、Y和Z各自独立为卤素原子、羟基、甲酰基、可能被取代的烷基、可能被取代的烷氧基、烷硫基、烷基亚磺酰基、烷基亚磺酰基或类似基团,A为羰基、硫羰基、亚烷基或单键,R1和R2各自独立为氢原子、可能被取代的烷基、可能被取代的烯基、可能被取代的炔基、可能被取代的芳基、甲酰基、烷基羰基、氰基或类似基团,而m和n各自独立为0、1、2、3或4。
  • Substituted thiazole derivatives bearing 3-pyridyl groups, process for preparing the same and use thereof
    申请人:——
    公开号:US20040072876A1
    公开(公告)日:2004-04-15
    The present invention provides a pharmaceutical composition having a steroid C 17,20 -lyase inhibitory activity, which is useful as a prophylactic or therapeutic agent of prostatism, tumor such as breast cancer and the like, more particularly, a steroid C 17,20 -lyase inhibitor containing a compound represented by the formula: 1 wherein A 1 is an aromatic hydrocarbon group optionally having substituents or a heterocyclic group optionally having substituents, one of A 2 and A 3 is a hydrogen atom, a halogen atom, a C 1-4 aliphatic hydrocarbon group optionally having substituents or an optionally esterified carboxyl group, the other of A 2 and A 3 is an aromatic hydrocarbon group optionally having substituents or a heterocyclic group optionally having substituents, and at least one of A 1 , A 2 and A 3 is a 3-pyridyl group optionally having substituents, or a salt thereof or a prodrug thereof.
    本发明提供了一种具有类固醇C17,20-裂解酶抑制活性的药物组合物,其可作为前列腺增生症、乳腺癌等肿瘤的预防或治疗剂,更具体地,是一种含有以下化合物的类固醇C17,20-裂解酶抑制剂:式中,A1为芳香族碳氢基团,可选地具有取代基,或者为杂环基团,可选地具有取代基;A2和A3中的一个为氢原子、卤素原子、C1-4脂肪族碳氢基团,可选地具有取代基,或者为可选酯化的羧基;另一个为芳香族碳氢基团,可选地具有取代基,或者为杂环基团,可选地具有取代基;且A1、A2和A3中至少有一个为可选地具有取代基的3-吡啶基团,或其盐或前药。
  • Biphenyl derivative or its salt, and pesticide containing it as an active ingredient
    申请人:Mitani Shigeru
    公开号:US20070135497A1
    公开(公告)日:2007-06-14
    A pesticide having stabilized high pesticidal effects for crop plants infected with plant diseases, is presented. The pesticide contains a biphenyl derivative represented by the formula (I) or its salt, as an active ingredient: wherein X, Y and Z are each independently a halogen atom, a hydroxyl group, a formyl group, an alkyl group which may be substituted, an alkoxy group which may be substituted, an alkylthio group, an alkylsulfonyl group, an alkylsulfinyl group, or the like, A is a carbonyl group, a thiocarbonyl group, an alkylene group, or a single bond, R 1 and R 2 are each independently a hydrogen atom, an alkyl group which may be substituted, an alkenyl group which may be substituted, an alkynyl group which may be substituted, an aryl group which may be substituted, a formyl group, an alkylcarbonyl group, a cyano group, or the like, and m and n are each independently 0, 1, 2, 3 or 4.
    提供了一种稳定高杀虫效果的杀虫剂,用于感染植物病害的作物。该杀虫剂包含一种双苯衍生物,其由式(I)或其盐表示,作为活性成分:其中X、Y和Z各自独立地是卤素原子、羟基、甲酰基、可被取代的烷基、可被取代的烷氧基、烷基硫基、烷基磺酰基、烷基亚磺酰基或类似的基团,A是羰基、硫代羰基、烷基烯基或单键,R1和R2各自独立地是氢原子、可被取代的烷基、可被取代的烯基、可被取代的炔基、可被取代的芳基、甲酰基、烷基羰基、氰基或类似的基团,m和n各自独立地为0、1、2、3或4。
  • SUBSTITUTED THIAZOLE DERIVATIVES BEARING 3-PYRIDYL GROUPS, PROCESS FOR PREPARING THE SAME AND USE THEREOF
    申请人:Takeda Pharmaceutical Company Limited
    公开号:EP1348706B1
    公开(公告)日:2009-08-19
  • BIPHENYL DERIVATIVE OR ITS SALT, AND PESTICIDE CONTAINING IT AS AN ACTIVE INGREDIENT
    申请人:ISHIHARA SANGYO KAISHA, LTD.
    公开号:EP1681924A1
    公开(公告)日:2006-07-26
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同类化合物

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