3-溴-5-氟苄醇 | 216755-56-5

• 物质功能分类: 有机原料 - 有机氟化合物 - 氟苄醇系列
• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 3-溴-5-氟苄醇
• 中文别名: 3-溴-5-氟苯甲醇
• 英文名称: (3-bromo-5-fluorophenyl)methanol
• 英文别名: 3-bromo-5-fluorobenzyl alcohol；5-fluoro-3-hydroxymethylbromobenzene
• CAS: 216755-56-5
• 化学式: C₇H₆BrFO
• mdl: MFCD04116320
• 分子量: 205.026
• InChiKey: KQWBQTOZXPPFIY-UHFFFAOYSA-N

物化性质

• 沸点：
  259.0±25.0 °C(Predicted)
• 密度：
  1.658±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  10
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.142
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  2

安全信息

• 危险品标志：
  Xi
• 安全说明：
  S26,S36
• 危险类别码：
  R36/37/38
• 海关编码：
  2906299090
• 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：
  室温且干燥

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
3-Bromo-5-fluorobenzyl alcohol
Product Name:
Synonyms:

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Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.
H315: Causes skin irritation
H319: Causes serious eye irritation
H335: May cause respiratory irritation
P261: Avoid breathing dust/fume/gas/mist/vapours/spray
Wear protective gloves/protective clothing/eye protection/face protection
P280:
P305+P351+P338: IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present
and easy to do – continue rinsing
P304+P340: IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing
P405: Store locked up

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Section 3. Composition/information on ingredients.
3-Bromo-5-fluorobenzyl alcohol
Ingredient name:
CAS number: 216755-56-5

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

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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.

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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.

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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.
Storage: Store in closed vessels, refrigerated.

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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.

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Section 9. Physical and chemical properties
Not specified
Appearance:
Boiling point: No data
Melting point: No data
Flash point: No data
Density: No data
Molecular formula: C7H6BrFO
Molecular weight: 205

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

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Section 11. Toxicological information
No data.

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Section 12. Ecological information
No data.

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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.

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Section 14. Transportation information
Non-harzardous for air and ground transportation.

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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.

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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
  3-溴-5-氟苯甲酸	3-bromo-5-fluorobenzoic acid	176548-70-2	C7H4BrFO2	219.01
  3-溴-5-氟苯甲醛	3-bromo-5-fluorobenzaldehyde	188813-02-7	C7H4BrFO	203.011

• 下游产品

  中文名称	英文名称	CAS号	化学式	分子量
  3-溴-5-氟苯甲醛	3-bromo-5-fluorobenzaldehyde	188813-02-7	C7H4BrFO	203.011
  3-氟-5-溴溴苄	1-bromo-3-(bromomethyl)-5-fluorobenzene	216755-57-6	C7H5Br2F	267.923
  2-(3-溴-5-氟苯基)乙腈	2-(3-bromo-5-fluorophenyl)acetonitrile	305800-58-2	C8H5BrFN	214.037

反应信息

• 作为反应物：
  描述：

  3-溴-5-氟苄醇 在 manganese(IV) oxide 作用下， 生成 3-溴-5-氟苯甲醛
  参考文献：
  名称：

  新型二取代的含苯基的3,4-二氨基-3-环丁烯-1,2-二酮作为CXCR2受体拮抗剂的合成及构效关系。

  摘要：

  合成了一系列的3,4-和3,5-二取代的含苯基环丁烯二酮类似物，并将其评估为CXCR2受体拮抗剂。苯环解离模式的变化提供了在低纳摩尔范围内具有有效CXCR2结合亲和力的新化合物。此外，两种有效的化合物19和26表现出良好的口服药代动力学特征。

  DOI：

  10.1016/j.bmcl.2008.02.010
• 作为产物：
  描述：

  3-溴-5-氟苯甲酸 在 硼烷四氢呋喃络合物 作用下， 以 四氢呋喃 为溶剂， 以95%的产率得到3-溴-5-氟苄醇
  参考文献：
  名称：

  Nivasorexant （ACT-539313） 的发现：在临床试验中研究的第一个选择性食欲素-1 受体拮抗剂 （SO1RA）

  摘要：

  食欲素系统由两种神经肽（食欲素 A 和 B）和两种受体（OX1 和 OX2）组成。选择性 OX1 受体拮抗剂 （SO1RA） 因其在治疗 CNS 疾病（包括药物滥用、进食、强迫症或焦虑症）方面的潜在用途而受到关注。虽然阻断 OX2 会降低觉醒度，但选择性拮抗 OX1 的预期优势是能够在不促进睡眠的情况下实现临床疗效。在本文中，我们报告了我们从双重食欲素受体拮抗剂开始的发现工作，并描述了一个偶然的发现，该发现触发了药物化学程序，最终鉴定出有效的 SO1RA ACT-539313。在时间表诱导的烦渴大鼠模型中的疗效支持选择该化合物作为临床前候选化合物的决定。Nivasorexant （20） 是第一个进入临床开发的 SO1RA，并于 2022 年完成了暴食症的首个概念验证 II 期临床试验。

  DOI：

  10.1021/acs.jmedchem.3c01894

文献信息

• [EN] TETRAZOLINONE COMPOUNDS AND ITS USE AS PESTICIDES<br/>[FR] COMPOSÉS DE TÉTRAZOLINONE ET LEUR UTILISATION EN TANT QUE PESTICIDES
  申请人：SUMITOMO CHEMICAL CO

  公开号：WO2013162072A1

  公开（公告）日：2013-10-31

  The present invention provides a compound having an excellent efficacy for controlling pests. A tetrazolinone compound of a formula (1): [wherein R1 represents an C6-C16 aryl group, an C1-C12 alkyl group, or a C3-C12 cycloalkyl group, etc., which each optionally be substituted; R2, R3, R4 and R5 represent independently of each other a hydrogen atom, a halogen atom or an C1-C3 alkyl group, etc.; R6 represents an C1-C6 alkyl group, a C3-C6 cycloalkyl group, a halogen atom, a C1-C6 haloalkyl group, an C2-C6 alkenyl group, an C1-C6 alkoxy group, or a C1-C6 haloalkoxy group, etc.; R7, R8 and R9 represent independently of each other a hydrogen atom, a halogen atom, or an C1-C4 alkyl group, etc.; X represents an oxygen atom or a sulfur atom; and R10 represents an C1-C6 alkyl group, etc.] shows an excellent controlling efficacy on pests.

  本发明提供了一种具有优异杀虫效果的化合物。公式（1）的四唑酮化合物：[其中R1代表C6-C16芳基、C1-C12烷基或C3-C12环烷基等，每个都可以选择性地被取代；R2、R3、R4和R5分别独立地代表氢原子、卤素原子或C1-C3烷基等；R6代表C1-C6烷基、C3-C6环烷基、卤素原子、C1-C6卤代烷基、C2-C6烯基、C1-C6烷氧基或C1-C6卤代烷氧基等；R7、R8和R9分别独立地代表氢原子、卤素原子或C1-C4烷基等；X代表氧原子或硫原子；R10代表C1-C6烷基等]在杀虫方面表现出优异的控制效果。
• Aminoheteroaryl benzamides as kinase inhibitors
  申请人：Bagdanoff Jeffrey T.

  公开号：US09242996B2

  公开（公告）日：2016-01-26

  The present invention provides a compound of Formula (I) or a salt thereof; and therapeutic uses of these compounds. The present invention further provides pharmaceutical compositions comprising these compounds, and compositions comprising these compounds with a therapeutic co-agent.

  本发明提供了化合物的化合物（I）或其盐； 以及这些化合物的治疗用途。本发明还提供了包含这些化合物的药物组合物，以及包含这些化合物与治疗辅助剂的组合物。
• [EN] N3-SUBSTITUTED IMINOPYRIMIDINONES AS RENIN INHIBITORS, COMPOSITIONS, AND THEIR USE<br/>[FR] IMINOPYRIMIDINONES SUBSTITUÉES EN N3 EN TANT QU'INHIBITEURS DE LA RÉNINE, COMPOSITIONS ET LEUR UTILISATION
  申请人：MERCK SHARP & DOHME

  公开号：WO2013142396A1

  公开（公告）日：2013-09-26

  In its many embodiments, the present invention provides provides certain N3-substituted iminopyrimidinones of Formula (I): and tautomers and stereoisomers thereof, and pharmaceutically acceptable salts of said compounds, said tautomeros and said stereoisomers, wherein each of the variables shown in the formula are as defined herein. The novel compounds of the invention are useful as renin inhibitors and/or for the treatment and prevention of various pathologies related thereto, including cardiovascular events, hypertension, and renal insufficiency. Pharmaceutical compositions comprising one or more such compounds (alone and in combination with one or more other active agents), and methods for their preparation and use, are also disclosed.

  在其多种实施方式中，本发明提供了以下式（I）的某些N3-取代的咪唑嘧啶酮化合物及其互变异构体和立体异构体，以及所述化合物的药学上可接受的盐，所述互变异构体和所述立体异构体，其中所示的各变量如本文所定义。本发明的新化合物可用作肾素抑制剂和/或用于治疗和预防与之相关的各种病理，包括心血管事件、高血压和肾功能不全。还公开了包括一种或多种这样的化合物（单独和与一种或多种其他活性剂的组合）的药物组合物，以及其制备和使用方法。
• [EN] HETEROCYCLYL PYRAZOLOPYRIMIDINE ANALOGUES AS JAK INHIBITORS<br/>[FR] ANALOGUES D'HÉTÉROCYCLYL PYRAZOLOPYRIMIDINE EN TANT QU'INHIBITEURS DE JAK
  申请人：CELLZOME LTD

  公开号：WO2011048082A1

  公开（公告）日：2011-04-28

  The present invention relates to compounds of formula (I) wherein X1 to X5, Y, Z1 to Z3, and R have the meaning as cited in the description and the claims. Said compounds are useful as JAK inhibitors 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X1至X5，Y，Z1至Z3和R的含义如描述和权利要求中所述。所述化合物可用作JAK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性疾病。该发明还涉及包括所述化合物的药物组合物，以及制备这类化合物以及用作药物的用途。
• [EN] SUBSTITUTED AROMATIC COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS FOR THE PREVENTION AND TREATMENT OF OSTEOPOROSIS<br/>[FR] COMPOSÉS AROMATIQUES SUBSTITUÉS ET COMPOSITIONS PHARMACEUTIQUES POUR LA PRÉVENTION ET LE TRAITEMENT DE L'OSTÉOPOROSE
  申请人：PROMETIC BIOSCIENCES INC

  公开号：WO2016054728A1

  公开（公告）日：2016-04-14

  The present invention concerns the use of compounds for preventing and/or treating osteoporosis, for stimulating bone formation, for stimulating bone remodeling, for stimulating the differentiation and mineralization of osteoblasts, for inhibiting bone resorption and for modulating serum level of adiponectin in a subject. These uses have been found for compounds represented by Formula I and pharmaceutically acceptable salts thereof. wherein A is C5 alkyl, C6 alkyl, C5 alkenyl, C6 alkenyl, C(O)-(CH2)n-CH3 or CH(OH)-(CH2)n-CH3 wherein n is 3 or 4; R1 is H, F or OH; R2 is H, F, OH, C6 alkyl, C5 alkenyl, C6 alkenyl, C(O)-(CH2)n-CH3 or CH(OH)-(CH2)n-CH3 wherein n is 3 or 4; R3 is H, F, OH or CH2Ph; R4 is H, F, or OH; Q is 1) (CH2)mC(O)OH wherein m is 1 or 2, 2) CH(F)-C(O)OH, 3) CF2-C(O)OH or 4) C(O)-C(O)OH.

  本发明涉及用于预防或治疗骨质疏松症、刺激骨骼形成、刺激骨骼重塑、刺激成骨细胞的分化和矿化、抑制骨吸收以及调节受试者血清中脂联素水平的化合物的用途。已经发现，这些用途适用于由公式I表示的化合物及其药用可接受的盐。其中A是C5烷基、C6烷基、C5烯基、C6烯基、C(O)-(CH2)n-CH3或CH(OH)-(CH2)n-CH3，其中n是3或4；R1是H、F或OH；R2是H、F、OH、C6烷基、C5烯基、C6烯基、C(O)-(CH2)n-CH3或CH(OH)-(CH2)n-CH3，其中n是3或4；R3是H、F、OH或CH2Ph；R4是H、F或OH；Q是1) (CH2)mC(O)OH，其中m是1或2，2) CH(F)-C(O)OH，3) CF2-C(O)OH或4) C(O)-C(O)OH。