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4-碘氰基砒啶 | 913836-19-8

中文名称
4-碘氰基砒啶
中文别名
4-碘-2-吡啶甲腈
英文名称
4-iodo-2-cyanopyridine
英文别名
4-iodopicolinonitrile;4-iodopyridine-2-carbonitrile;2-cyano-4-iodopyridine
4-碘氰基砒啶化学式
CAS
913836-19-8
化学式
C6H3IN2
mdl
——
分子量
230.008
InChiKey
BGDBXTAJJAFSGO-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

  • 熔点:
    67-69
  • 沸点:
    301.7±27.0 °C(Predicted)
  • 密度:
    2.04±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.6
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    36.7
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 危险品标志:
    Xi
  • 海关编码:
    2933399090
  • 储存条件:
    保持冷静

SDS

SDS:a0b3b9fe62bfec5a2e0c1753eedbc64c
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 4-Iodopicolinonitrile
Synonyms: 4-Iodo-2-cyanopyridine

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.
H302: Harmful if swallowed
H315: Causes skin irritation
H318: Causes serious eye damage
H335: May cause respiratory irritation
P261: Avoid breathing dust/fume/gas/mist/vapours/spray
P280: Wear protective gloves/protective clothing/eye protection/face protection
P305+P351+P338: IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present
and easy to do – continue rinsing

Section 3. Composition/information on ingredients.
Ingredient name: 4-Iodopicolinonitrile
CAS number: 913836-19-8

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.
Storage: Store in closed vessels, refrigerated.

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
Not specified
Appearance:
Boiling point: No data
Melting point: No data
Flash point: No data
Density: No data
Molecular formula: C6H3IN2
Molecular weight: 230.0

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 Iodide.

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

反应信息

  • 作为反应物:
    描述:
    4-碘氰基砒啶甲醇 、 sodium tetrahydroborate 、 nickel(II) chloride hexahydrate 、 sodium hydride 作用下, 以 N,N-二甲基甲酰胺 、 mineral oil 为溶剂, 反应 2.33h, 生成 tert-butyl (4-isobutoxypyridin-2-yl)methylcarbamate
    参考文献:
    名称:
    [EN] PHENYL- SULFONYL DERIVATIVES AS MEDIATORS OF TRPA1 RECEPTOR ACTIVITY FOR THE TREATMENT OF PAIN
    [FR] DÉRIVÉS DE PHÉNYLSULFONYLE EN TANT QUE MÉDIATEURS DE L'ACTIVITÉ DE RÉCEPTEUR TRPA1 POUR LE TRAITEMENT DE LA DOULEUR
    摘要:
    式I的化合物,其中A和R1-R7如索权中所定义,表现出TRPA1活性,并且作为TRPA1调节剂是有用的。
    公开号:
    WO2012152983A1
  • 作为产物:
    描述:
    4-溴吡啶-2-甲腈copper(l) iodide 、 sodium iodide 、 N,N'-二甲基乙二胺 作用下, 以 1,4-二氧六环 为溶剂, 反应 20.0h, 以2.5 g的产率得到4-碘氰基砒啶
    参考文献:
    名称:
    [EN] BENZYL-, (PYRIDIN-3-YL)METHYL- OR (PYRIDIN-4-YL)METHYL-SUBSTITUTED OXADIAZOLOPYRIDINE DERIVATIVES AS GHRELIN O-ACYL TRANSFERASE (GOAT) INHIBITORS
    [FR] DÉRIVÉS D'OXADIAZOLOPYRIDINE À SUBSTITUTION BENZYLE, (PYRIDIN-3-YL)MÉTHYLE OU (PYRIDIN-4-YL)MÉTHYLE UTILISÉS EN TANT QU'INHIBITEURS DE LA GHRÉLINE O-ACYLTRANSFÉRASE (GOAT)
    摘要:
    本发明涉及一般式(I)的化合物,其中基团R1和R2的定义如权利要求1中所述,该化合物具有有价值的药理特性,特别是与胃饥饿素O-酰基转移酶(GOAT)结合并调节其活性。这些化合物适用于治疗和预防可以受到该受体影响的疾病,如代谢性疾病,特别是肥胖症。
    公开号:
    WO2019149657A1
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文献信息

  • [EN] PYRIDINE COMPOUND, PESTICIDAL COMPOSITION AND METHOD OF CONTROLLING PEST<br/>[FR] COMPOSÉ DE PYRIDINE, COMPOSITION PESTICIDE ET PROCÉDÉ DE LUTTE CONTRE LES NUISIBLES
    申请人:SUMITOMO CHEMICAL CO
    公开号:WO2009066786A1
    公开(公告)日:2009-05-28
    A pyridine compound represented by the following general formula (1); the pyridine compound in which R1 is a C1-C3 fluoroalkyl group or a C1-C3 fluoroalkoxy group; the pyridine compound in which R2 is a hydrogen atom; the pyridine compound in which R2 is a group represented by Q1; a pesticidal composition containing the pyridine compound as an active ingredient; and a method of controlling a pest including applying an effective amount of the pyridine compound to the pest or a place where the pest inhabits, are provided.
    以下是通用公式(1)表示的吡啶化合物;其中R1是C1-C3氟烷基或C1-C3氟烷氧基的吡啶化合物;其中R2是氢原子的吡啶化合物;其中R2是由Q1表示的基团的吡啶化合物;包含所述吡啶化合物作为活性成分的杀虫剂组合物;以及一种控制害虫的方法,包括向害虫或害虫栖息地施加有效量的吡啶化合物。
  • WNT SIGNALING INHIBITOR
    申请人:KYOWA HAKKO KIRIN CO., LTD.
    公开号:US20160168125A1
    公开(公告)日:2016-06-16
    A Wnt signaling inhibitor which comprises, as an active ingredient, a fused-ring heterocyclic compound represented by the following formula (IA) or a pharmaceutically acceptable salt thereof, and the like are provided: (wherein, n 1A represents 0 or 1; n 2A and n 3A may be the same or different, and each represents 1 or 2; R OA represents optionally substituted aryl or the like; R 2A represents a hydrogen atom or the like; R 3A represents an optionally substituted aromatic heterocyclic group or the like; X 1A , X 2A , X 3A and X 4A each represent CH or the like; Y 1A represents CH 2 or the like; Y 2A represents N or the like; and L A represents CH 2 or the like).
    提供一种Wnt信号抑制剂,其包括以下式(IA)所表示的融合环杂环化合物作为活性成分或其药学上可接受的盐等:(其中,n1A表示0或1;n2A和n3A可以相同也可以不同,每个表示1或2;ROA表示可选择地取代的芳基或类似物;R2A表示氢原子或类似物;R3A表示可选择地取代的芳香杂环基或类似物;X1A、X2A、X3A和X4A各自表示CH或类似物;Y1A表示CH2或类似物;Y2A表示N或类似物;LA表示CH2或类似物)。
  • [EN] CERTAIN CHEMICAL ENTITIES, COMPOSITIONS AND METHODS<br/>[FR] ENTITÉS CHIMIQUES, COMPOSITIONS ET PROCÉDÉS
    申请人:INTELLIKINE INC
    公开号:WO2009088986A1
    公开(公告)日:2009-07-16
    Chemical entities that modulate PD kinase activity, pharmaceutical compositions containing the chemical entities, and methods of using these chemical entities for treating diseases and conditions associated with P13 kinase activity are described herein.
    本文描述了调节PD激酶活性的化学实体,含有这些化学实体的药物组合物,以及使用这些化学实体治疗与P13激酶活性相关的疾病和症状的方法。
  • [EN] INHIBITORS OF THE RENAL OUTER MEDULLARY POTASSIUM CHANNEL<br/>[FR] INHIBITEURS DU CANAL POTASSIQUE MÉDULLAIRE EXTERNE RÉNAL
    申请人:MERCK SHARP & DOHME
    公开号:WO2015017305A1
    公开(公告)日:2015-02-05
    The present invention provides compounds of Formula I and the pharmaceutically acceptable salts thereof, which are inhibitors of the ROMK (Kir1.1) channel. The compounds may be used as diuretic and/or natriuretic agents and for the therapy and prophylaxis of medical conditions including cardiovascular diseases such as hypertension, heart failure and chronic kidney disease and conditions associated with excessive salt and water retention.
    本发明提供了式I的化合物及其药学上可接受的盐,这些化合物是ROMK(Kir1.1)通道的抑制剂。这些化合物可用作利尿剂和/或钠利尿剂,并用于治疗和预防包括高血压、心力衰竭和慢性肾病在内的心血管疾病以及与过多盐分和水分潴留有关的疾病。
  • [EN] METABOTROPIC GLUTAMATE RECEPTOR MODULATORS<br/>[FR] MODULATEURS DES RÉCEPTEURS MÉTABOTROPES AU GLUTAMATE
    申请人:MERZ PHARMA GMBH & CO KGAA
    公开号:WO2012052451A1
    公开(公告)日:2012-04-26
    The invention relates to heterocyclic derivatives of formula (I) as well as their pharmaceutically acceptable salts. The invention further relates to a process for the preparation of such compounds. The compounds of the invention are mGluR5 modulators and are therefore useful for the control and prevention of acute and/or chronic neurological disorders wherein Y, W, R1, R2 and R3 are as defined in claim 1.
    该发明涉及公式(I)的杂环衍生物及其药学上可接受的盐。该发明还涉及制备这类化合物的方法。该发明的化合物是mGluR5调节剂,因此对于控制和预防急性和/或慢性神经系统疾病是有用的,其中Y、W、R1、R2和R3如权利要求1中所定义。
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