E50604
Ethyltriphenylphosphonium bromide
99%
Manufacturer: Sigma Aldrich
CAS Number: 1530-32-1
Synonym(S): TEP
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 25 G | E50604-25-G | In Stock | ₹ 3,864.53 |
| 100 G | E50604-100-G | In Stock | ₹ 11,214.70 |
E50604 - 25 G
In Stock
Quantity
1
Base Price: ₹ 3,864.53
GST (18%): ₹ 695.615
Total Price: ₹ 4,560.145
Quality Level
200
Assay
99%
reaction suitability
reaction type: C-C Bond Formation
mp
203-205 °C (lit.)
SMILES string
[Br-].CC[P+](c1ccccc1)(c2ccccc2)c3ccccc3
InChI
1S/C20H20P.BrH/c1-2-21(18-12-6-3-7-13-18,19-14-8-4-9-15-19)20-16-10-5-11-17-20;/h3-17H,2H2,1H3;1H/q+1;/p-1
InChI key
JHYNXXDQQHTCHJ-UHFFFAOYSA-M
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Sigma Aldrich Fine Chemicals Biosciences Ethyltriphenylphosphonium bromide 99% | 1530-32-1 | MFCD00011838 | 100G | Sigma Aldrich Fine Chemicals Biosciences | ₹ 14,359.53 | |
| | Sigma Aldrich Fine Chemicals Biosciences Ethyltriphenylphosphonium bromide 99% | 1530-32-1 | MFCD00011838 | 25G | Sigma Aldrich Fine Chemicals Biosciences | ₹ 5,484.40 | |
 | 1530-32-1 | Ethyltriphenylphosphonium bromide | A2B Chem | ₹ 1,540.08 - ₹ 14,031.84 |
Related Products
Description
- Application: Reactant for synthesis of: D-amino acids from L-cysteine-derived thiazolidinesLeiodolide A via aldol reactions and Horner-Wadsworth-Emmons olefinationCycloalkanoindolines via diastereoselective intramolecular inimo-ene reactionsWXYZA′ domain of maitotoxin using the coupling of key building blocksReactant for: Solid-state metathesis polycondensation to form alkyl-dipropenylthiophene monomersMizoroki-Heck cyclization and cascading Tsuji-Trost cyclization / lactonization cyclization reactions for synthesis of an ABC ring system
SAFETY INFORMATION
Pictograms
Signal Word
Danger
Hazard Statements
Precautionary Statements
P264 - P273 - P280 - P301 + P310 - P305 + P351 + P338 - P405
Hazard Classifications
Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1
WGK
WGK 2
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Compare Similar Items
Show Difference
Quality Level: 200
Assay: 99%
reaction suitability: reaction type: C-C Bond Formation
mp: 203-205 °C (lit.)
SMILES string: [Br-].CC[P+](c1ccccc1)(c2ccccc2)c3ccccc3
InChI: 1S/C20H20P.BrH/c1-2-21(18-12-6-3-7-13-18,19-14-8-4-9-15-19)20-16-10-5-11-17-20;/h3-17H,2H2,1H3;1H/q+1;/p-1
InChI key: JHYNXXDQQHTCHJ-UHFFFAOYSA-M
Quality Level:
200
Assay:
99%
reaction suitability:
reaction type: C-C Bond Formation
mp:
203-205 °C (lit.)
SMILES string:
[Br-].CC[P+](c1ccccc1)(c2ccccc2)c3ccccc3
InChI:
1S/C20H20P.BrH/c1-2-21(18-12-6-3-7-13-18,19-14-8-4-9-15-19)20-16-10-5-11-17-20;/h3-17H,2H2,1H3;1H/q+1;/p-1
InChI key:
JHYNXXDQQHTCHJ-UHFFFAOYSA-M
Quality Level: 100
Assay: 97%
reaction suitability: __
mp: 87-90 °C (lit.)
SMILES string: CCNC(N)=O
InChI: 1S/C3H8N2O/c1-2-5-3(4)6/h2H2,1H3,(H3,4,5,6)
InChI key: RYECOJGRJDOGPP-UHFFFAOYSA-N
Quality Level:
100
Assay:
97%
reaction suitability:
__
mp:
87-90 °C (lit.)
SMILES string:
CCNC(N)=O
InChI:
1S/C3H8N2O/c1-2-5-3(4)6/h2H2,1H3,(H3,4,5,6)
InChI key:
RYECOJGRJDOGPP-UHFFFAOYSA-N
Quality Level: 200
Assay: 97%
reaction suitability: __
mp: __
SMILES string: CCC(=O)C=C
InChI: 1S/C5H8O/c1-3-5(6)4-2/h3H,1,4H2,2H3
InChI key: __
Quality Level:
200
Assay:
97%
reaction suitability:
__
mp:
__
SMILES string:
CCC(=O)C=C
InChI:
1S/C5H8O/c1-3-5(6)4-2/h3H,1,4H2,2H3
InChI key:
__
Quality Level: 300
Assay: 99.0-101.0% (titration)
reaction suitability: reagent type: chelator
mp: 248 °C (dec.) (lit.)
SMILES string: __
InChI: __
InChI key: __
Quality Level:
300
Assay:
99.0-101.0% (titration)
reaction suitability:
reagent type: chelator
mp:
248 °C (dec.) (lit.)
SMILES string:
__
InChI:
__
InChI key:
__