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牛磺酰胺盐酸盐 | 89756-60-5

中文名称
牛磺酰胺盐酸盐
中文别名
——
英文名称
taurinamide hydrochloride
英文别名
2-aminoethanesulfonamide hydrochloride;2-aminoethane-1-sulfonamide hydrochloride;β-aminoethanesulfonamide hydrochloride;2-aminoethylsulfonamide hydrochloride;2-aminoethanesulphonamide hydrochloride;2-aminoethanesulfonamide;hydron;chloride
牛磺酰胺盐酸盐化学式
CAS
89756-60-5
化学式
C2H8N2O2S*ClH
mdl
MFCD02258341
分子量
160.625
InChiKey
DGUVEYAZTOUCEJ-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:
    133 °C
  • 溶解度:
    DMSO(轻微)、甲醇(轻微、加热)、水(轻微)

计算性质

  • 辛醇/水分配系数(LogP):
    -2.18
  • 重原子数:
    8
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    94.6
  • 氢给体数:
    3
  • 氢受体数:
    4

安全信息

  • 海关编码:
    2935009090
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319
  • 储存条件:
    室温且干燥环境下使用。

SDS

SDS:0d08f82a170ee06b70fbf757abc9cfef
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 2-Aminoethanesulfonamide, HCl
Synonyms:

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.
H335: May cause respiratory irritation
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: 2-Aminoethanesulfonamide, HCl
CAS number: 89756-60-5

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.

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
Melting point: No data
Flash point: No data
Density: No data
Molecular formula: C2H8N2O2S.ClH
Molecular weight: 160.6

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, sulfur oxides.

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:
    牛磺酰胺盐酸盐 、 sodium nitrite 作用下, 生成 2-羟基-1-磺酰胺
    参考文献:
    名称:
    [EN] OXATHIAZINE DERIVATIVES AS ANTIBACTERIAL AND ANTICANCER AGENTS
    [FR] DÉRIVÉS D'OXATHIAZINE À TITRE D'AGENTS ANTIBACTÉRIENS ET ANTICANCÉREUX
    摘要:
    新的类似于氧硫唑的化合物及其衍生物可作为抗肿瘤和抗微生物药物使用。
    公开号:
    WO2013190355A1
  • 作为产物:
    描述:
    2-formamidoethylsulfonamide盐酸 作用下, 以 乙醚 为溶剂, 反应 3.0h, 以87%的产率得到牛磺酰胺盐酸盐
    参考文献:
    名称:
    4-(Substituted Anilino)-Quinazoline Derivatives Useful as Tyrosine Kinase Inhibitors
    摘要:
    本发明涉及作为酪氨酸激酶抑制剂的4-(取代苯胺基)-喹唑啉衍生物。具体地,公开了式I的化合物,或其药学上可接受的盐或溶剂化合物,其中式I中的每个取代基在描述中有定义。还公开了式I化合物的制备方法,药物组合物以及其药用。式I化合物是有效的酪氨酸激酶抑制剂。
    公开号:
    US20120208833A1
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文献信息

  • [EN] MACROCYLIC PYRIDINE DERIVATIVES<br/>[FR] DÉRIVÉS DE PYRIDINE MACROCYCLIQUES
    申请人:JANSSEN PHARMACEUTICA NV
    公开号:WO2015150557A1
    公开(公告)日:2015-10-08
    The present invention relates to substituted macrocylic pyrimidine derivatives of Formula (I) wherein the variables have the meaning defined in the claims. The compounds according to the present invention have EF2K inhibitory activity and optionally also Vps34 inhibitory activity. The invention further relates to processes for preparing such novel compounds, pharmaceutical compositions comprising said compounds as an active ingredient as well as the use of said compounds as a medicament.
    本发明涉及式(I)的取代大环嘧啶衍生物,其中变量的含义如权利要求中所定义。根据本发明的化合物具有EF2K抑制活性,还可能具有Vps34抑制活性。本发明还涉及制备这种新化合物的方法,包含所述化合物作为活性成分的药物组合物,以及将所述化合物用作药物的用途。
  • SULFONE AMIDE LINKED BENZOTHIAZOLE INHIBITORS OF ENDOTHELIAL LIPASE
    申请人:BRISTOL-MYERS SQUIBB COMPANY
    公开号:US20160326125A1
    公开(公告)日:2016-11-10
    The present invention provides compounds of Formula (I) as defined in the specification and compositions comprising any of such novel compounds. These compounds are endothelial lipase inhibitors which may be used medicaments.
    本发明提供了规范中定义的Formula (I)的化合物以及包含任何此类新化合物的组合物。这些化合物是内皮酶抑制剂,可用作药物。
  • [EN] NAPHTHYRIDINE DERIVATIVES AS INHIBITORS OF HYPOXIA INDUCIBLE FACTOR (HIF) HYDROXYLASE<br/>[FR] DÉRIVÉS DE NAPHTHYRIDINE EN TANT QU'INHIBITEURS D'UN FACTEUR INDUCTIBLE PAR L'HYPOXIE
    申请人:FIBROGEN INC
    公开号:WO2012106472A1
    公开(公告)日:2012-08-09
    The present disclosure relates to novel compounds, methods, and compositions capable of inhibiting HIF hydroxylase enzyme activity, thereby increasing the stability and/or activity of hypoxia inducible factor (HIF).
    本公开涉及能够抑制HIF羟化酶活性的新化合物、方法和组合物,从而增加缺氧诱导因子(HIF)的稳定性和/或活性。
  • [EN] IMIDAZOLE DERIVATIVES AND THEIR USE IN THE TREATMENT OF AUTOIMMUNE OR INFLAMMATORY DISEASES OR CANCERS<br/>[FR] DÉRIVÉS D'IMIDAZOLE ET LEUR UTILISATION DANS LE TRAITEMENT DE MALADIES AUTO-IMMUNES OU INFLAMMATOIRES OU DE CANCERS
    申请人:GLAXOSMITHKLINE IP NO 2 LTD
    公开号:WO2018041964A1
    公开(公告)日:2018-03-08
    Compounds of formula (I) and salts thereof: wherein R1, R2, R3, a, X1, X2, X3, X4, and X5 are as defined hereinbefore. Compounds of formula (I) and salts thereof have been found to inhibit the binding of the BET family of bromodomain containing proteins to, for example, acetylated lysine residues and thus may have use in therapy, for example in the treatment of autoimmune and inflammatory diseases, such as rheumatoid arthritis; and cancers.
    化合物的化学式(I)及其盐:其中R1、R2、R3、a、X1、X2、X3、X4和X5的定义如前所述。已发现化合物的化学式(I)及其盐能够抑制BET家族溴结构域蛋白与例如乙酰化赖氨酸残基的结合,因此可能在治疗中发挥作用,例如在治疗自身免疫和炎症性疾病(如类风湿性关节炎)和癌症方面。
  • [EN] AMIDE, UREA OR SULFONE AMIDE LINKED BENZOTHIAZOLE INHIBITORS OF ENDOTHELIAL LIPASE<br/>[FR] INHIBITEURS DE LIPASE ENDOTHÉLIALE À BASE DE BENZOTHIAZOLE LIÉS À UNE AMINE, L'URÉE OU UN SULFONE AMIDE
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2014015088A1
    公开(公告)日:2014-01-23
    The present invention provides compounds of Formula (I): as defined in the specification and compositions comprising any of such novel compounds. These compounds are endothelial lipase inhibitors which may be used as medicaments.
    本发明提供了如规范中定义的Formula (I)的化合物,以及包含任何此类新化合物的组合物。这些化合物是内皮脂酶抑制剂,可用作药物。
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