1,2-Bis(chlorodimethylsilyl)ethane

HCID 83552

Basic information

CAS
13528-93-3
Standard SMILES
C[Si](C)(Cl)CC[Si](C)(C)Cl
InChIKey
VGQOKOYKFDUPPJ-UHFFFAOYSA-N
Molecular formula
C6H16Cl2Si2
Average molar mass
215.26 g/mol
Monoisotopic mass
214.016759

Names & identifiers

Preferred name
1,2-Bis(chlorodimethylsilyl)ethane
IUPAC
chloro-[2-[chloro(dimethyl)silyl]ethyl]-dimethylsilane
English name
1,2-Bis(chlorodimethylsilyl)ethane
Molecular formula
C6H16Cl2Si2
Molecular weight
215.27

Names & synonyms

1,2-Bis(chlorodimethylsilyl)ethane13528-93-3Ethylenebis(chlorodimethylsilane)Silane, 1,2-ethanediylbis[chlorodimethyl-B4OCJ0E6J11,1,4,4-Tetramethyl-1,4-dichlorodisilethylene1,2-bis(dimethylchlorosilyl)ethaneEINECS 236-871-0Silane, 1,2-ethanediylbis(chlorodimethyl-Silane, 1,1'-(1,2-ethanediyl)bis(1-chloro-1,1-dimethyl-DTXSID9065520LS-7080
Show more names
1,1,4,4-TETRAMETHYL-1,4-DICHLORODISILYLETHYLENE1,2-Bis(chlorodimethylsilyl)DK065DK525STABASESILANE BM2E[-CH2Si(CH3)2Cl]21,2-Bis(dimethylchlorosily)ethane1,2-Bis(chlorodimethylsily)ethane
ETHYLENEBIS[CHLORODIMETHYLSILANE]1,2-BIS(CHLORODIMETHYLSILYL)ETHANE [MI]2,5-DIMETHYL-2,5-DICHLORO-2,5-DISILAHEXANESilane, 1,1'-(1,2-ethanediyl)bis[1-chloro-1,1-dimethyl-RefChem:411388DTXCID0034306236-871-0chloro[2-(chlorodimethylsilyl)ethyl]dimethylsilane

Database identifiers

CAS
13528-93-3
PubChem CID
83552
DTXSID
DTXSID9065520
UNII
B4OCJ0E6J1
EC Number
236-871-0
Nikkaji
J241.167I

Properties

Computed structural properties

Topological polar surface area
0 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
0
Rotatable bonds
3
Heavy atoms
10

Physicochemical properties

Melting point
35 · 35-38 °C (lit.)
Boiling point
198 °C/734 · 198 °C/734 mmHg (lit.)
Density
0.99 · 0.99
Flash point
155 °F · 155 °F
storage temp.
Inert atmosphere,Room Temperature
form
Low Melting Solid

Safety & regulation

GHS classification

GHS Classification · 5 items

Danger

H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]

P260, P264, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P363, 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.;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.

Hazard information

Regulatory InformationChemical: Silane, 1,2-ethanediylbis[chlorodimethyl-
Hazard Classes and CategoriesSkin Corr. 1B (100%)

Regulatory information

Regulatory InformationChemical: Silane, 1,2-ethanediylbis[chlorodimethyl-

Safety data

F
10-21
PPE
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
wgk
3
tsca
TSCA listed
ridadr
UN 3261 8/PG 2
hs_code
29319000

Chemistry & industry

Uses & manufacturing

General Manufacturing InformationSilane, 1,1'-(1,2-ethanediyl)bis[1-chloro-1,1-dimethyl-: ACTIVE
Applications · 2 items

Uses1,2-Bis(chlorodimethylsilyl)ethane is used as Protecting Reagent for Primary Amines. It is also used in Medicine field, electronics industry and polymer material.

Uses1,2-Bis(chlorodimethylsilyl)ethane can be used as a reagent for the protection of primary amines as their tetramethyldisilylazacyclopentane or Stabase adducts; used in combination with zinc to form organozinc carbenoids; electrophilic silylating reagent.Protection of Primary Amines.Few protecting groups exist for the N,N-diprotection of primary amines. The tetramethyldisilylazacyclopentane or Stabase adduct (3) is particularly attractive for this purpose due to its ease of preparation, base stability and facile removal. This cyclic disilane is easily prepared (eq 1) from the commercially available title reagent (1).For primary amines with pKa values between 10 and 11, typical reaction conditions involve the treatment of a dichloromethane solution of the amine with (1) in the presence of two equivalents of triethylamine at room temperature. Subsequent workup with aqueous dihydrogen phosphate provides (3) in excellent yields.1 Stabase adducts are quite stable to strongly basic conditions such as n-butyllithium and s-butyllithium (at 25°C), lithium diisopropylamide, and Grignard reagents making it a superb candidate for use in the alkylation of substrates bearing a primary amine. For example, protected amino acid derivatives are easily alkylated (eq 2).After formation of the lithium enolate of the protected ethyl glycinate (4) under standard conditions, exposure to various alkyl halides or aldehydes yields alkylation products such as (5).

Suppliers100 total

梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
郑州阿尔法化工有限公司+86-18530059196 · [email protected]
苏州道澜生物医药科技有限公司15952404857 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
湖北科孚乐材料科技有限公司027-84459282 13720265353 · [email protected]

Related reactions

66 records

Compound notes

Loading…