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
Show more names
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
- Formal charge
- 0
- Complexity
- 98
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
- color
- Transparent
- Water Solubility
- Reacts with water.
- Sensitive
- Moisture Sensitive
- Hydrolytic Sensitivity
- 8 · 8: reacts rapidly with moisture, water, protic solvents
- BRN
- 1920141 · 1920141
- InChI
- 1S/C6H16Cl2Si2/c1-9(2,7)5-6-10(3,4)8/h5-6H2,1-4H3
- InChIKey
- VGQOKOYKFDUPPJ-UHFFFAOYSA-N
- SMILES
- C[Si](C)(Cl)CC[Si](C)(C)Cl
- CAS DataBase Reference
- 13528 · 13528-93-3(CAS DataBase Reference)
- FDA UNII
- 4 OCJ0E6J1 · B4OCJ0E6J1
- EPA Substance Registry System
- 1 · Silane, 1,2-ethanediylbis[chlorodimethyl- (13528-93-3)
- UNSPSC Code
- 12352101 · 12352101
- NACRES
- 22 · NA.22
- Symbol(GHS)
- 5 · GHS05
- Signal word
- Danger
- Hazard statements
- 314 · H314
- Precautionary statements
- 260 · P260-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338-P363
- PPE
- 3 · Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
- Hazard Codes
- C
- Risk Statements
- 34 · 34-10
- Safety Statements
- 26 · 26-28-36/37/39-45-16
- RIDADR
- 3261 · UN 3261 8/PG 2
- WGK Germany
- 3 · 3
- F
- 10 · 10-21
- TSCA
- TSCA listed
- HazardClass
- 8 · 8
- PackingGroup
- III
- HS Code
- 29319000 · 29319000
- Storage Class
- 8 A · 8A - Combustible corrosive hazardous materials
- Hazard Classifications
- 1 B · Skin Corr. 1B
Safety & regulation
GHS classification
GHS Classification
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 information
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
- risk_code
- 34-10
- Signal word
- Danger
- Symbol(GHS)
- GHS05
- hazard_code
- C
- safety_code
- 26-28-36/37/39-45-16
- hazard_class
- 8
- Storage Class
- 8A - Combustible corrosive hazardous materials
- packing_group
- III
- Hazard statements
- H314
- Hazard Classifications
- Skin Corr. 1B
- Precautionary statements
- P260-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338-P363
Chemistry & industry
Uses & manufacturing
Applications
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).
Upstream & downstream products
Downstream products
Suppliers100 total
Related reactions
Compound notes
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