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2-氯-4,5-二甲氧基苯胺 | 32829-09-7

中文名称
2-氯-4,5-二甲氧基苯胺
中文别名
——
英文名称
2-chloro-4,5-dimethoxyaniline
英文别名
——
2-氯-4,5-二甲氧基苯胺化学式
CAS
32829-09-7
化学式
C8H10ClNO2
mdl
MFCD08691143
分子量
187.626
InChiKey
LRNKEBRHHZJMCX-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):
    1.8
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    44.5
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2922299090

SDS

SDS:eb500037736528b594c529ffeaa4e3a9
查看
Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 2-Chloro-4,5-dimethoxyaniline
Synonyms:

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

Section 3. Composition/information on ingredients.
Ingredient name: 2-Chloro-4,5-dimethoxyaniline
CAS number: 32829-09-7

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: C8H10ClNO2
Molecular weight: 187.6

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.

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:
    2-氯-4,5-二甲氧基苯胺 以57%的产率得到
    参考文献:
    名称:
    PETERS W.; PIOTROWSKA H.; SERAFIN B.; URBANSKI T., POL. J. PHARMACOL. PHARM., 1975, 27, NO 3, 289-295,
    摘要:
    DOI:
  • 作为产物:
    描述:
    二甲氧基乙酰苯胺氯仿 、 alkali solution 、 作用下, 生成 2-氯-4,5-二甲氧基苯胺
    参考文献:
    名称:
    The Chemistry of Heterocyclic Quinones. I. The Direct Oxidation of 6-Hydroxycarbostyrils to Carbostyril-5,6-quinones
    摘要:
    DOI:
    10.1021/ja01638a031
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文献信息

  • [EN] AMIDO-SUBSTITUTED CYCLOHEXANE DERIVATIVES<br/>[FR] DÉRIVÉS DE CYCLOHEXANE À SUBSTITUTION AMIDO
    申请人:BAYER PHARMA AG
    公开号:WO2016177658A1
    公开(公告)日:2016-11-10
    The present invention relates to amido-substituted cyclohexane compounds of general formula (I), in which A, R4, R6, R7, R8, R9, R10 and R11 are as defined herein, to methods of preparing said compounds, to intermediate compounds useful for preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular of neoplasms, as a sole agent or in combination with other active ingredient.
    本发明涉及一般式(I)的酰胺取代环己烷化合物,其中A、R4、R6、R7、R8、R9、R10和R11如本文所定义,涉及制备所述化合物的方法,涉及用于制备所述化合物的中间化合物,涉及包含所述化合物的药物组合物和药物组合物,以及用于制造用于治疗或预防疾病的药物组合物的所述化合物的用途,特别是肿瘤,作为唯一药剂或与其他活性成分结合使用。
  • [EN] QUINAZOLINONE COMPOUNDS<br/>[FR] COMPOSÉS QUINAZOLINONE
    申请人:CEREPEUT INC
    公开号:WO2020176652A1
    公开(公告)日:2020-09-03
    New quinazolinone compounds are disclosed, as well as pharmaceutical compositions containing quinazolinones and methods for the treatment of diseases and conditions associated with mitochondrial dysfunction.
    揭示了新的喹唑啉酮化合物,以及含有喹唑啉酮的药物组合物和用于治疗与线粒体功能障碍相关的疾病和症状的方法。
  • PYRIMIDINE DERIVATIVES AS ZAP-70 INHIBITORS
    申请人:Ramsden Nigel
    公开号:US20120142667A1
    公开(公告)日:2012-06-07
    The invention relates to compounds of formula (I) wherein R 1 to R 5 , X and X 1 to X 3 have the meaning as cited in the description and the claims. Said compounds are useful as inhibitors of ZAP-70 for the treatment or prophylaxis of immunological, inflammatory, autoimmune, allergic disorders, and immunologically-mediated diseases. The invention also relates to pharmaceutical compositions including said compounds, the preparation of such compounds as well as the use as medicaments.
    本发明涉及式(I)的化合物,其中R1至R5、X和X1至X3的含义如描述和权利要求中所述。所述化合物可用作ZAP-70的抑制剂,用于治疗或预防免疫、炎症、自身免疫、过敏性疾病和免疫介导的疾病。本发明还涉及包括上述化合物的制药组合物,以及作为药物的用途和制备这种化合物的方法。
  • Farbfotografisches farbkupplerhaltiges Aufzeichnungsmaterial
    申请人:Agfa-Gevaert AG
    公开号:EP0122533A2
    公开(公告)日:1984-10-24
    Gelbkuppler der Formel worin bedeuten Y ein aromatischen, aliphatischen oder cycloaliphatischen Rest; X Wasserstoff oder eine abspaltbare Gruppe; R' Halogen; R2, R' Alkyl mit je 1 bis 20 C-Atomen, sind gut in Ölbildnern löslich und kuppeln mit hoher Farbausbeute. Sie sind stabil gegen Wärme und Feuchtigkeit und liefern bei der Farbentwicklung stabile gelbe Farbstoffe mit einem Absorptionsmaximum unterhalb von 450 nm. Sie haben ein hohes Absorptionsvermögen im nahen UV-Bereich und sind gegen Schwankungen des pH-Wertes bei der Verarbeitung praktisch unempfindlich.
    黄色耦合器的公式为 其中平均值 Y 是芳香族、脂肪族或环脂族自由基 X 是氢或可拆分基团 R' 是卤素; R2、R' 烷基各含 1 至 20 个 C 原子、 易溶于油形成剂,并具有较高的成色率。它们对热和湿度稳定,在显色过程中可提供稳定的黄色染料,吸收最大值低于 450 纳米。它们在近紫外线范围内有很高的吸收能力,对加工过程中的 pH 值波动几乎不敏感。
  • Oxidation dyeing process using a composition comprising a monoaminobenzene and a metal catalyst
    申请人:L'OREAL
    公开号:US10251827B2
    公开(公告)日:2019-04-09
    The invention relates to a process for dyeing keratin fibers, comprising the use of one or more metal catalysts and of a composition (A) comprising: —one or more oxidizing agents, and —at least one monoaminobenzene of formula (I), or an addition salt or solvate thereof in which the radicals R1 to R5 represent, independently of each other: a hydrogen atom; a halogen atom, a C1-C6 alkyl radical, a C1-C6 alkoxy radical, a carboxylic radical (—COOH), a sulfonic radical (—S03 H); two of the adjacent radicals R1 to R5 possibly forming, with the carbon atoms that bear them, a saturated or unsaturated 5- to 7-membered ring, optionally comprising from 1 to 2 heteroatoms, preferably oxygen, the said ring being optionally fused with a saturated or unsaturated 5- to 6-membered ring; on condition that at least one of the radicals R1 to R5 represents an optionally substituted alkoxy radical and preferably at least one of the other radicals R1 to R5 is a hydrogen atom.
    本发明涉及一种角蛋白纤维染色工艺,包括使用一种或多种金属催化剂和一种组合物(A),组合物(A)包括: -一种或多种氧化剂,和 -至少一种式(I)的单胺苯,或其加成盐或溶液,其中自由基 R1 至 R5 各自代表:氢原子、卤素原子、C1-C6 烷基、C1-C6 烷氧基、羧基 (-COOH)、磺酸基 (-S03 H);R1 至 R5 中相邻的两个基团可与含有它们的碳原子形成饱和或不饱和的 5 至 7 元环,可选择包含 1 至 2 个杂原子,最好是氧,所述环可选择与饱和或不饱和的 5 至 6 元环融合;条件是 R1 至 R5 自由基中至少有一个代表任选取代的烷氧基,且 R1 至 R5 自由基中至少有一个是氢原子。
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