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3', 5'-二氯-2, 2, 2-三氟苯乙酮 | 130336-16-2

中文名称
3', 5'-二氯-2, 2, 2-三氟苯乙酮
中文别名
3',5'-二氯-2,2,2-三氟苯乙酮;3,5-二氯-2,2,2-三氟苯乙酮;3,5-二氯-2`,2`,2`-三氟苯乙酮;3,5-二氯三氟乙酰基苯;1-(3,5-二氯)-2,2,2-三氟苯乙酮
英文名称
3,5-dichloro-2,2,2-trifluoroacetophenone
英文别名
1-(3,5-dichlorophenyl)-2,2,2-trifluoroethanone;1-(3,5-dichlorophenyl)-2,2,2-trifluoroethan-1-one;3,5-dichloro-trifluoroacetophenone;α,α,α-trifluoro-3,5-dichloroacetophenone;3’,5’-dichloro-2,2,2-trifluoroacetophenone;3',5'-Dichloro-2,2,2-trifluoroacetophenone
3', 5'-二氯-2, 2, 2-三氟苯乙酮化学式
CAS
130336-16-2
化学式
C8H3Cl2F3O
mdl
MFCD01319996
分子量
243.012
InChiKey
DZDSQRPDUCSOQV-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

  • 沸点:
    265℃
  • 密度:
    1.506
  • 闪点:
    114℃
  • 溶解度:
    乙腈(微溶)、氯仿(微溶)、甲醇(微溶)

计算性质

  • 辛醇/水分配系数(LogP):
    4
  • 重原子数:
    14
  • 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:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    4

安全信息

  • 安全说明:
    S26,S36/37/39
  • 危险类别码:
    R36/37/38
  • 海关编码:
    2914700090
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335
  • 储存条件:
    适宜在室温和干燥的环境中保存。

SDS

SDS:ad90888d006febbf5420d68dbf32b20e
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 1-(3,5-Dichlorophenyl)-2,2,2-trifluoroethanone
Synonyms:

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

Section 3. Composition/information on ingredients.
Ingredient name: 1-(3,5-Dichlorophenyl)-2,2,2-trifluoroethanone
CAS number: 130336-16-2

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: C8H3Cl2F3O
Molecular weight: 243.0

Section 10. Stability and reactivity
Conditions to avoid: Heat, flames and sparks.
Materials to avoid: Oxidizing agents.
Possible hazardous combustion products: Carbon monoxide, hydrogen chloride, hydrogen fluoride.

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

制备方法与用途

用途

随着光敏树脂在电子工业、印刷工业、涂料、粘合剂和医疗材料中的广泛应用,对光聚合光敏树脂的光引发剂研究日益受到关注。其中,3',5'-二氯-2,2,2-三氟苯乙酮是一种重要的光引发剂。此外,它还可用于制造肥皂和香烟。

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:
    3', 5'-二氯-2, 2, 2-三氟苯乙酮 在 sodium tetrahydroborate 作用下, 以 甲醇 为溶剂, 反应 2.0h, 以79%的产率得到1-(3,5-dichlorophenyl)-2,2,2-trifluoroethanol
    参考文献:
    名称:
    [EN] PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO
    [FR] COMPOSITIONS PESTICIDES ET LEURS PROCÉDÉS ASSOCIÉS
    摘要:
    这份文件揭示了具有以下化学式(“化学式一”)的分子以及相关的工艺。
    公开号:
    WO2014100206A1
  • 作为产物:
    描述:
    盐酸 作用下, 以85.3%的产率得到3', 5'-二氯-2, 2, 2-三氟苯乙酮
    参考文献:
    名称:
    一种三氟苯乙酮衍生物的制备方法
    摘要:
    本申请涉及有机合成领域,更具体地说,它涉及一种三氟苯乙酮衍生物的制备方法,以取代苯胺为原料,经重氮化反应、偶联反应和水解反应三步,完成三氟苯乙酮衍生物的制备。该制备方法工艺简单,收率较高,反应整体产生的三废较少,适用于工业大规模生产。
    公开号:
    CN113461503A
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文献信息

  • [EN] AZOLINE COMPOUNDS<br/>[FR] COMPOSÉS AZOLINE
    申请人:BASF SE
    公开号:WO2015128358A1
    公开(公告)日:2015-09-03
    The present invention relates to azoline compounds of formula (I) wherein A, B1, B2, B3, G1, G2, X1, R1, R3a, R3b, Rg1 and Rg2 are as defined in the claims and the description. The compounds are useful for combating or controlling invertebrate pests, in particular arthropod pests and nematodes. The invention also relates to a method for controlling invertebrate pests by using these compounds and to plant propagation material and to an agricultural and a veterinary composition comprising said compounds.
    本发明涉及式(I)的噁唑啉化合物,其中A、B1、B2、B3、G1、G2、X1、R1、R3a、R3b、Rg1和Rg2如权利要求和描述中所定义。这些化合物对抗或控制无脊椎动物害虫,特别是节肢动物害虫和线虫方面具有用途。该发明还涉及一种利用这些化合物控制无脊椎动物害虫的方法,以及包括所述化合物的植物繁殖材料、农业和兽医组合物。
  • [EN] ISOXAZOLINE DERIVATIVES AS INSECTICIDES<br/>[FR] DÉRIVÉS D'ISOXAZOLINE EN TANT QU'INSECTICIDES
    申请人:SYNGENTA PARTICIPATIONS AG
    公开号:WO2011101402A1
    公开(公告)日:2011-08-25
    The present invention relates to compounds formula (I), wherein P is P1, P2, heterocyclyl or heterocyclyl substituted by one to five Z; and wherein A1, A2, A3, A4, G1, R1, R2, R3, R4, R5, R6, R17, R18, R19 and R20 are as defined in claim 1; or a salt or N-oxide thereof. Furthermore, the present invention relates to processes and intermediates for preparing compounds of formula (I), to insecticidal, acaricidal, nematicidal and molluscicidal compositions comprising the compounds of formula (I) and to methods of using the compounds of formula (I) to control insect, acarine, nematode and mollusc pests.
    本发明涉及化合物式(I),其中P为P1、P2、杂环烷基或被一到五个Z取代的杂环烷基;以及其中A1、A2、A3、A4、G1、R1、R2、R3、R4、R5、R6、R17、R18、R19和R20如权利要求1中所定义;或其盐或N-氧化物。此外,本发明涉及制备化合物式(I)的过程和中间体,包括化合物式(I)的杀虫剂、杀螨剂、杀线虫剂和杀软体动物剂组合物,以及使用化合物式(I)控制昆虫、螨虫、线虫和软体动物害虫的方法。
  • ISOXAZOLINE DERIVATIVES AS INSECTICIDES
    申请人:Pitterna Thomas
    公开号:US20120316124A1
    公开(公告)日:2012-12-13
    The present invention relates to compounds formula (I), wherein P is P1, P2, heterocyclyl or heterocyclyl substituted by one to five Z; and wherein A 1 , A 2 , A 3 , A 4 , G 1 , R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 17 , R 18 , R 19 and R 20 are as defined in claim 1 ; or a salt or N-oxide thereof. Furthermore, the present invention relates to processes and intermediates for preparing compounds of formula (I), to insecticidal, acaricidal, nematicidal and molluscicidal compositions comprising the compounds of formula (I) and to methods of using the compounds of formula (I) to control insect, acarine, nematode and mollusc pests.
    本发明涉及化合物式(I),其中P为P1、P2、杂环烷基或被1至5个Z取代的杂环烷基;以及其中A1、A2、A3、A4、G1、R1、R2、R3、R4、R5、R6、R17、R18、R19和R20如权利要求1所定义;或其盐或N-氧化物。此外,本发明涉及制备化合物式(I)的过程和中间体,包括化合物式(I)的杀虫剂、杀螨剂、杀线虫剂和杀软体动物剂组合物,以及使用化合物式(I)控制昆虫、螨虫、线虫和软体动物害虫的方法。
  • [EN] ISOXAZOLINE COMPOUNDS AND THEIR USE AS PEST CONTROL AGENTS<br/>[FR] COMPOSÉS ISOXAZOLINE ET LEUR UTILISATION EN TANT QU'AGENTS DE LUTTE CONTRE LES ORGANISMES NUISIBLES
    申请人:PI INDUSTRIES LTD
    公开号:WO2021038501A1
    公开(公告)日:2021-03-04
    The present invention discloses an isoxazoline compound of formula (I), wherein, R1, R2a, R2b, R2c, A, T and Z are as defined in the detailed description. The present invention further discloses methods for preparation of compounds of formula (I) and use of the compounds of formula (I) as a pest control agents.
    本发明公开了一种式(I)的异氧杂环烷化合物,其中,R1、R2a、R2b、R2c、A、T和Z如详细说明中所定义。本发明还公开了制备式(I)化合物的方法以及将式(I)化合物用作杀虫剂的用途。
  • 一种3`,5`-二氯-2,2,2-三氟苯乙酮的合成方法
    申请人:台州臻挚生物科技有限公司
    公开号:CN112028752B
    公开(公告)日:2023-02-03
    本申请涉及化工制药的技术领域,尤其是涉及一种3',5'‑二氯‑2,2,2‑三氟苯乙酮的合成方法,通过先将1,3,5‑三氯苯或3,5‑二氯‑1‑溴苯与镁反应形成格氏试剂在于三氟乙酰基试剂发生亲核加成反应,经酸处理后得到3',5'‑二氯‑2,2,2‑三氟苯乙酮,其反应条件温和,原料成本低廉,具有较好的经济效应和广泛的工业化生产前景。
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