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三甲基(苯基硒代甲基)硅烷 | 56253-60-2

中文名称
三甲基(苯基硒代甲基)硅烷
中文别名
(苯基锡甲基)三甲基硅烷
英文名称
trimethyl-phenylselanylmethyl-silane
英文别名
Phenylselenotrimethylsilylmethane;phenylselenomethyltrimethylsilane;Trimethyl[(phenylseleno)methyl]silane;(phenylselenomethyl)trimethylsilane;Phenylselenomethyltrimethylsilan;Trimethyl((phenylseleno)methyl)silane;trimethyl(phenylselanylmethyl)silane
三甲基(苯基硒代甲基)硅烷化学式
CAS
56253-60-2
化学式
C10H16SeSi
mdl
MFCD00042834
分子量
243.283
InChiKey
QXFASNHOOXGHDD-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:
    106 °C6 mm Hg(lit.)
  • 密度:
    1.176 g/mL at 25 °C(lit.)
  • 闪点:
    >230 °F
  • 稳定性/保质期:
    遵照规定使用和储存,则不会发生分解。

计算性质

  • 辛醇/水分配系数(LogP):
    4.06
  • 重原子数:
    12
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

安全信息

  • TSCA:
    No
  • 危险等级:
    6.1(b)
  • 危险品标志:
    T,N
  • 安全说明:
    S20/21,S28,S45,S60,S61
  • 危险类别码:
    R50/53,R23/25,R33
  • WGK Germany:
    3
  • 危险品运输编号:
    UN 2810 6.1/PG 3
  • 包装等级:
    III
  • 危险类别:
    6.1(b)

SDS

SDS:737a0b1bc469500f088bcfae775872bb
查看
Version 1.2
Regulation (EC) No 1907/2006

1 - Product and Company Information

Product Name (PHENYLSELENOMETHYL)TRIMETHYLSILANE, 99%

2 - Hazards Identification

SPECIAL INDICATION OF HAZARDS TO HUMANS AND THE ENVIRONMENT
Toxic by inhalation and if swallowed. Danger of cumulative
effects. Very toxic to aquatic organisms, may cause long-term
adverse effects in the aquatic environment.

3 - Composition/Information on Ingredients

Product Name CAS # EC no Annex I
Index Number
(PHENYLSELENOMETHYL)TRIMETHYLSILAN 56253-60-2 260-077-3 034-002-00-8
E
Formula C10H16SeSi
Molecular Weight 243,2900 AMU

4 - First Aid Measures

AFTER INHALATION
If inhaled, remove to fresh air. If not breathing give
artificial respiration. If breathing is difficult, give oxygen.
AFTER SKIN CONTACT
In case of contact, immediately wash skin with soap and copious
amounts of water.
AFTER EYE CONTACT
In case of contact, immediately flush eyes with copious amounts
of water for at least 15 minutes.
AFTER INGESTION
If swallowed, wash out mouth with water provided person is
conscious. Call a physician.

5 - Fire Fighting Measures
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EXTINGUISHING MEDIA
Suitable: Water spray. Carbon dioxide, dry chemical powder, or
appropriate foam.
SPECIAL RISKS
Specific Hazard(s): Emits toxic fumes under fire conditions.
SPECIAL PROTECTIVE EQUIPMENT FOR FIREFIGHTERS
Wear self-contained breathing apparatus and protective clothing
to prevent contact with skin and eyes.

6 - Accidental Release Measures

PROCEDURE(S) OF PERSONAL PRECAUTION(S)
Wear respirator, chemical safety goggles, rubber boots, and
heavy rubber gloves.
METHODS FOR CLEANING UP
Cover with dry lime or soda ash, pick up, keep in a closed
container, and hold for waste disposal. Ventilate area and wash
spill site after material pickup is complete.

7 - Handling and Storage

HANDLING
Directions for Safe Handling: Do not breathe vapor. Avoid
contact with eyes, skin, and clothing.
STORAGE
Conditions of Storage: Keep tightly closed. Store in a cool dry
place.

8 - Exposure Controls / Personal Protection

ENGINEERING CONTROLS
Safety shower and eye bath. Mechanical exhaust required.
GENERAL HYGIENE MEASURES
Wash thoroughly after handling. Wash contaminated clothing before
reuse.
PERSONAL PROTECTIVE EQUIPMENT
Respiratory Protection: Use respirators and components tested and
approved under appropriate government standards such as NIOSH (US)
or CEN (EU). Where risk assessment shows air-purifying respirators
are appropriate use a full-face respirator with multi-purpose
combination (US) or type ABEK (EN 14387) respirator cartridges as
a backup to engineering controls. If the respirator is the sole
means of protection, use a full-face supplied air respirator.
Hand Protection: Compatible chemical-resistant gloves.
Eye Protection: Chemical safety goggles.

9 - Physical and Chemical Properties

Appearance Color: Deep yellow-green
Form: Clear liquid
Property Value At Temperature or Pressure
ALDRICH www.molbase.com
pH N/A
BP/BP Range 106,000 °C 6,000 mmHg
MP/MP Range N/A
Flash Point 95,000 °C Method: closed cup
Flammability N/A
Autoignition Temp N/A
Oxidizing Properties N/A
Explosive Properties N/A
Explosion Limits N/A
Vapor Pressure N/A
SG/Density 1,1760 g/cm3
Partition Coefficient N/A
Viscosity N/A
Vapor Density N/A
Saturated Vapor Conc. N/A
Evaporation Rate N/A
Bulk Density N/A
Decomposition Temp. N/A
Solvent Content N/A
Water Content N/A
Surface Tension N/A
Conductivity N/A
Miscellaneous Data N/A
Solubility N/A

10 - Stability and Reactivity

STABILITY
Materials to Avoid: Strong oxidizing agents.
HAZARDOUS DECOMPOSITION PRODUCTS
Hazardous Decomposition Products: Carbon monoxide, Carbon dioxide,
Silicon oxide, Selenium/selenium oxides.

11 - Toxicological Information

SIGNS AND SYMPTOMS OF EXPOSURE
To the best of our knowledge, the chemical, physical, and
toxicological properties have not been thoroughly investigated.
ROUTE OF EXPOSURE
Multiple Routes: May be harmful by inhalation, ingestion, or
skin absorption. May cause irritation.
TARGET ORGAN INFORMATION
Liver.

12 - Ecological Information

No data available.

13 - Disposal Considerations

SUBSTANCE DISPOSAL
Dissolve or mix the material with a combustible solvent and burn
in a chemical incinerator equipped with an afterburner and
scrubber. Observe all federal, state, and local environmental
regulations.

14 - Transport Information
ALDRICH www.molbase.com

RID/ADR
UN#: 2810
Class: 6.1
PG: III
Proper Shipping Name: Toxic liquid, organic, n.o.s.
IMDG
UN#: 2810
Class: 6.1
PG: III
Proper Shipping Name: Toxic liquid, organic, n.o.s.
Marine Pollutant: No
Severe Marine Pollutant: No
Technical Name: Required
IATA
UN#: 2810
Class: 6.1
PG: III
Proper Shipping Name: Toxic liquid, organic, n.o.s.
Inhalation Packing Group I: No
Technical Name: Required

15 - Regulatory Information

CLASSIFICATION AND LABELING ACCORDING TO EU DIRECTIVES
ANNEX I INDEX NUMBER: 034-002-00-8
NOTA: A
INDICATION OF DANGER: T-N
Toxic. Dangerous for the environment.
R-PHRASES: 23/25-33-50/53
Toxic by inhalation and if swallowed. Danger of cumulative
effects. Very toxic to aquatic organisms, may cause long-term
adverse effects in the aquatic environment.
S-PHRASES: 20/21-28-45-60-61
When using do not eat, drink, or smoke. After contact with
skin, wash immediately with plenty of soap-suds. In case of
accident or if you feel unwell, seek medical advice immediately
(show the label where possible). This material and its
container must be disposed of as hazardous waste. Avoid release
to the environment. Refer to special instructions/safety data
sheets.
COUNTRY SPECIFIC INFORMATION
Germany
WGK: 3
Self-Classification

16 - Other Information

WARRANTY
The above information is believed to be correct but does not
purport to be all inclusive and shall be used only as a guide. The
information in this document is based on the present state of our
knowledge and is applicable to the product with regard to
appropriate safety precautions. It does not represent any
guarantee of the properties of the product. Inc.,
shall not be held liable for any damage resulting from handling or
ALDRICH www.molbase.com
from contact with the above product. See reverse side of invoice
or packing slip for additional terms and conditions of sale.
Copyright 2010 Co. License granted to make
unlimitedpaper copies for internal use only.
DISCLAIMER
For R&D use only. Not for drug, household or other uses.
ALDRICH www.molbase.com


SECTION 16 - ADDITIONAL INFORMATION
N/A



反应信息

  • 作为反应物:
    描述:
    三甲基(苯基硒代甲基)硅烷sodium 作用下, 以 叔丁醇 为溶剂, 生成 二苯基二硒醚
    参考文献:
    名称:
    苯基硒烷的苯基硒键的光还原裂解
    摘要:
    从三乙胺到苯硒代链烷烃的光诱导电子转移可导致PhSe键的选择性还原和裂解,从而导致苯和相应的二烯化烯基硒基自由基的形成。
    DOI:
    10.1016/0040-4039(94)88021-2
  • 作为产物:
    描述:
    2,2,3,3,4,4,4-Heptafluoro-1-phenylselanylbutan-1-ol氯甲基三甲基硅烷1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下, 以 四氢呋喃 为溶剂, 反应 0.5h, 以54%的产率得到三甲基(苯基硒代甲基)硅烷
    参考文献:
    名称:
    1-(Organoselanyl)perfluoroalkanols: A Stable and Efficient Precursor for Organoselenols
    摘要:
    成功制备了 1-(有机硒基)全氟烷醇 1、3、4 和 10,并与己酰氯反应生成了相应的酯 5、7 和 8 以及硒酯 6。在 DBU 介导下,七氟丁醇 4、10 和 α-对硝基苯甲酸酯 2 与烷基卤化物发生烷基化反应,很容易就能得到烷基苯基硒化物 9a-9i 和 11a-11c,收率从好到高。
    DOI:
    10.1246/cl.2008.1046
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文献信息

  • gem-Heterosubstituted (stannyl)methylsilanes as synthetic equivalents of functionalized α-stannyl(methyl) anions
    作者:Damiano Tanini、Tiziano Nocentini、Antonella Capperucci
    DOI:10.24820/ark.5550190.p011.038
    日期:——
    Received mm-dd-yyyy Accepted mm-dd-yyyy Published on line mm-dd-yyyy Dates to be inserted by editorial office Abstract α-Heterosubstituted silyl derivatives, such as phenylthio-, phenylselenoand benzotriazolyl-stannyl silanes, react with aldehydes under TBAF catalysis, leading to α-substituted-β-hydroxy stannanes, able to behave as precursors of Zand E-olefins, generated by deoxystannylation. This
    收到 mm-dd-yyyy 接受 mm-dd-yyyy 在线发布 mm-dd-yyyy 编辑部插入的日期 摘要 α-杂取代的甲硅烷基衍生物,如苯硫基、苯基硒基和苯并三唑基-甲锡基硅烷,在 TBAF 下与醛反应催化,导致 α-取代-β-羟基锡烷,能够充当 Zand E-烯烃的前体,由脱氧锡烷基化产生。这种反应性表明这种杂取代的硅烷能够通过碳-硅键的温和官能化充当掩蔽的碳负离子。
  • The reactions of lithiobisphenylselenomethane with chloromethyltrimethylsilane and iodomethyltrimethylstannane: Novel 1,1 - and 1,2- elimination reactions in organoselenium/organotin chemistry
    作者:Tarun K. Sarkar、Tushar K. Satapathi
    DOI:10.1016/s0040-4039(00)99236-0
    日期:1989.1
    Anomalous and unprecedented 1,1- and 1,2-elimination reactions are reported in the alkylation of lithiobisphenylselenomethane 4 with chloromethyltrimethylsilane and iodomethyltrimethylstannane.
    据报道,在硫代双苯基硒代甲烷4与氯甲基三甲基硅烷和碘甲基三甲基锡烷的烷基化反应中,发生了异常且前所未有的1,1和1,2-消除反应。
  • (2,3)-1,2-epoxy-3-butanol. A useful synthon for the preparation of chiral 1,2-diols.
    作者:James D. White、Myung-chol Kang、Bernard G. Sheldon
    DOI:10.1016/s0040-4039(00)85949-3
    日期:1983.1
  • Transformation of α-phenylseleneketones to allylic selenides via migration of the phenylseleno group
    作者:Hisao Nishiyama、Kazuyoshi Itagaki、Noriyuki Osaka、Kenji Itoh
    DOI:10.1016/s0040-4039(00)88359-8
    日期:1982.1
  • Chadha, Raj K.; Chehayber, Jaafar M.; Drake, John E., Inorganic Chemistry, 1986, vol. 25, # 5, p. 611 - 615
    作者:Chadha, Raj K.、Chehayber, Jaafar M.、Drake, John E.
    DOI:——
    日期:——
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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cnmr
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐