基本情報
- 標準SMILES
C[Si](C)(C)N=[N+]=[N-]- InChIKey
SEDZOYHHAIAQIW-UHFFFAOYSA-N- 分子式
- C3H9N3Si
- 平均分子量
- 115.21 g/mol
概要
structure in first source
名称と識別子
- 優先名称
- Azidotrimethylsilane
- IUPAC
- azido(trimethyl)silane
- 現地名
- トリメチルシリルアジド
- 英語名
- Azidotrimethylsilane
- 分子式
- C3H9N3Si
- 分子量
- 115.21
名称と別名
名称をさらに表示
データベース識別子
- CAS
4648-54-8- PubChem CID
- 78378
- DTXSID
DTXSID3063542- UNII
- EM57JSM2Y9
- EC Number
- 225-078-5
- Nikkaji
- J80.870I
物性
構造計算による物性
- 極性表面積
- 14.4 Ų
- 水素結合供与体数
- 0
- 水素結合受容体数
- 2
- 回転可能結合数
- 1
- 重原子数
- 7
- 形式電荷
- 0
- 複雑度
- 97.2
実験および物理化学的性質
物理化学的性質
- 融点
- -95 °C · -95°C
- 沸点
- 92 · 92-95 °C(lit.)
- 比重(密度)
- 0.876 g/mL · 0.876 g/mL at 20 °C(lit.)
- 屈折率
- 20 · n20/D 1.415(lit.)
- 闪点
- 74 °F · 74 °F
- 貯蔵温度
- 2 · 2-8°C
- 溶解性
- トルエン、ジクロロメタン、エーテル、およびほとんどの有機溶媒と混和します。
- 外見
- 液体
- 比重
- 0.868 · 0.868
- 色
- 無色透明~微黄色透明
- 水溶解度
- 分解する
- BRN
- 1903730 · 1903730
- InChI
- 1S/C3H9N3Si/c1-7(2,3)6-5-4/h1-3H3
- InChIKey
- SEDZOYHHAIAQIW-UHFFFAOYSA-N
- SMILES
- C[Si](C)(C)N=[N+]=[N-]
- CAS データベース
- 4648 · 4648-54-8(CAS DataBase Reference)
- NISTの化学物質情報
- Azidotrimethylsilane(4648-54-8)
- EPAの化学物質情報
- Azidotrimethylsilane (4648-54-8)
化学的性質
化学的特性Azidotrimethylsilane (TMSN3) is a clear colorless to slightly yellow liquid. It shows very slow decomposition at high temperatures. It is a very commonly used azide source and has been used in the synthesis of aminotriazole ligands. Azidotrimethylsilane can be easily synthesised by adding chlorotrimethylsilane dropwise to a stirred solution of NaN3 in diethylene glycol dimethyl ether.
安全と法規制
GHS分類
GHS Classification
Danger
H225 (100%): Highly Flammable liquid and vapor [Danger Flammable liquids]
P210, P233, P240, P241, P242, P243, P261, P262, P264, P270, P271, P273, P280, P301+P316, P302+P352, P303+P361+P353, P304+P340, P316, P321, P330, P361+P364, P370+P378, P391, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 52 reports by companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
危険有害性情報
Regulatory Information
Chemical: Silane, azidotrimethyl-
Status: Active Update: 09-04-2018 https://echa.europa.eu/registration-dossier/-/registered-dossier/23688
Trimethylsilyl azide: Does not have an individual approval but may be used under an appropriate group standard
CSL Reaction Information
CSL00010
BORON TRIFLUORIDE + AZIDOTRIMETHYLSILANE
Combinations of TMSN3 and Lewis acids can detonate, presumably due to formation of HN3 from residual water. Avoid Lewis acids.
Explosive
Cycloaddition
User-Reported
安全データ
- F
- 10-33
- wgk
- 3
- tsca
- TSCA listed
- ridadr
- UN 1992 3/PG 2
- hs_code
- 29310095
- risk_code
- 11-23/24/25-50/53-29
- 安衛法
- 変異原性物質
- 消防法
- 危-4-2-III
- hazard_code
- F,T,N
- safety_code
- 16-36/37/39-45-8-57-36/37-29
- hazard_class
- 3
- packing_group
- II
- 自然発火温度
- 300 °C
- Hazard Classifications
- Acute Tox. 3 DermalAcute Tox. 3 InhalationAcute Tox. 3 OralFlam. Liq. 2
- ストレージクラス
- 3 - Flammable liquids
化学と産業
用途と製造
応用分野
用途有機合成原料。
使用Many applications of TMSA in organic synthesis have been reported but only representative examples are described herein.Substitution Reactions. Benzyl,allyl,and substituted alkyl halides are converted to the corresponding azides in 60–100% yields via reactions with TMSA under neutral conditions in a nonaqueous solvent (eq 1).By using tin(IV) chloride as a catalyst, secondary and tertiary cyclic and polycyclic halides are similarly transformed into the corresponding azides in 50–92% yields (eq 1).
調製方法
製造方法Azidotrimethylsilane may be synthesised by reacting trimethylchlorosilane with sodium azide in hexamethylphosphoramidic triamide. several methods for the synthesis of this azide have been reported.The procedure involving aluminum chloride is not recommended, since an explosive product is formed.Azidotrimethylsilane is now commercially available, and a representative synthetic procedure is as follows. A mixture of sodium azide and chlorotrimethylsilane is refluxed in di-n-butyl ether for 2 days and the azide is safely distilled directly from the reaction vessel. Purer compound (99% content) is obtained by redistillation of the product. Several improved conditions have been reported for the preparation of this azide.In these procedures, trimethylsilyl chloride is reacted with sodium azide either neat or in a high boiling point solvent, such as a mixture of silicone oil and polyethylene glycol. Distillation of the crude product usually provides trimethylsilyl azide (TMSA) in high purity (97.9%) and yield (97%).
純化方法Distil the azide through a Vigreux column (p 11) in a N2 atmosphere maintaining the oil bath temperature thermostat at 135-140o . Check the purity by 1H NMR [CHCl3, : single peak at 13cps from Me4Si]. Likely impurities are siloxane hydrolysis products. The azide is thermally stable even at 200o when it decomposes slowly without explosive violence. All the same, it is advisable to carry out the distillation behind a thick safety screen in a fumehood because unforseen EXPLOSIVE azides may be formed on long standing. [Birkofer & Wagner Org Synth Coll Vol VI 1030 1988.]
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