ビス(トリメチルシリル)スルフィド

Disilathiane, 1,1,1,3,3,3-hexamethyl-

HCID 76920

基本情報

CAS
3385-94-2
標準SMILES
C[Si](C)(C)S[Si](C)(C)C
InChIKey
RLECCBFNWDXKPK-UHFFFAOYSA-N
分子式
C6H18SSi2
平均分子量
178.44 g/mol
単同位体質量
178.06677482

名称と識別子

優先名称
Disilathiane, 1,1,1,3,3,3-hexamethyl-
IUPAC
trimethyl(trimethylsilylsulfanyl)silane
現地名
ビス(トリメチルシリル)スルフィド
英語名
BIS(TRIMETHYLSILYL) SULFIDE
分子式
C6H18SSi2
分子量
178.44

名称と別名

3385-94-2Bis(trimethylsilyl) sulfideHexamethyldisilathianeDisilathiane, hexamethyl-Disilthiane, hexamethyl-Disilathiane, 1,1,1,3,3,3-hexamethyl-EINECS 222-201-4NSC 252160DTXSID2063006RefChem:589178DTXCID0038756222-201-4
名称をさらに表示
ビス(トリメチルシリル)スルフィド1,1,1,3,3,3-ヘキサメチルプロパンジシラチアンヘキサメチルプロパンジシラチアンチオビス(トリメチルシラン)1,1,1,3,3,3-ヘキサメチルジシラチアンBIS(TRIMETHYLSILYL SULFIDE)ヘキサメチルジシルチアンヘキサメチルジシラチアンHexamethyldisilthianDK269athianehexamethyl-disilathianDisilthiane,hexamethyl-Hexamethyldisilylthiane
Bis(trimethylsilyl)sulfideHexamethyldisilthianetrimethyl(trimethylsilylsulfanyl)silane1,1,1,3,3,3-HexamethyldisilathianeMFCD00014851AZ6L5QJY5HNSC-252160Thiobis(trimethylsilane)

データベース識別子

CAS
3385-94-2
PubChem CID
76920
DTXSID
DTXSID2063006
UNII
AZ6L5QJY5H
EC Number
222-201-4
Nikkaji
J205.475B

物性

構造計算による物性

極性表面積
25.3 Ų
水素結合供与体数
0
水素結合受容体数
1
回転可能結合数
2
重原子数
9

実験および物理化学的性質

Kovats Retention Index993

物理化学的性質

沸点
164 °C · 164 °C(lit.)
比重(密度)
0.846 g/mL · 0.846 g/mL at 25 °C(lit.)
屈折率
20 · n20/D 1.4586(lit.)
闪点
79 °F · 79 °F
貯蔵温度
Flammables area
溶解性
テラヒドロフラン、トルエンと混和。

化学的性質

化学的特性clear colorless to slightly yellow liquid

安全と法規制

GHS分類

GHS Classification · 5 件

Danger

H226 (97.8%): Flammable liquid and vapor [Warning Flammable liquids];H301 (84.8%): Toxic if swallowed [Danger Acute toxicity, oral];H311 (84.8%): Toxic in contact with skin [Danger Acute toxicity, dermal];H315 (13%): Causes skin irritation [Warning Skin corrosion/irritation];H319 (13%): Causes serious eye irritation [Warning Serious eye damage/eye irritation];H331 (84.8%): Toxic if inhaled [Danger Acute toxicity, inhalation];H335 (13%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

P210, P233, P240, P241, P242, P243, P261, P262, P264, P264+P265, P270, P271, P280, P301+P316, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P316, P319, P321, P330, P332+P317, P337+P317, P361+P364, P362+P364, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 46 reports by companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.;Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.

危険有害性情報

Hazard Classes and CategoriesFlam. Liq. 3 (97.8%);Acute Tox. 3 (84.8%);Acute Tox. 3 (84.8%);Skin Irrit. 2 (13%);Eye Irrit. 2 (13%);Acute Tox. 3 (84.8%);STOT SE 3 (13%)

安全データ

F
10-13-21
wgk
3
tsca
TSCA listed
ridadr
UN 1993 3/PG 3
hs_code
29319090
risk_code
10-23/24/25

化学と産業

用途と製造

General Manufacturing InformationDisilathiane, 1,1,1,3,3,3-hexamethyl-: ACTIVE
応用分野 · 1 件

使用Bis(trimethylsilyl) sulfide (TMS2S) is used to reduce aromatic nitro groups to amines and the oxides of sulfur, selenium, and tellurium. Conditions for nitro group reduction (eq 1) are forcing; however, yields are good. Reactions of TMS2S with primary aliphatic nitro groups result in the formation of the thiohydroxamic acids (eq 2) which can be isolated or carried further to the nitrile. Secondary alkyl nitro derivatives provide oximes. Sulfoxides are reduced to sulfides, selenoxides to selenides, and telluroxides to tellurides. Conditions are mild and work well on both the aliphatic and aromatic oxides.

調製方法 · 1 件

純化方法Dissolve it in pet ether (b ca 40o), remove the solvent and distil it. Redistil it under atmospheric pressure of dry N2. It is collected as a colourless liquid which solidifies to a white solid in Dry-ice. On standing for several days it turns yellow possibly due to liberation of sulfur. Store it below 4o under dry N2. [Eaborn J Chem Soc 3077 1950, Beilstein 4 IV 4033.]

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関連反応

12 件

化合物ノート

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