696641
3,3-Dimethyl-1-(trifluoromethyl)-1,2-benziodoxole
95%
Manufacturer: Sigma Aldrich
CAS Number: 887144-97-0
Synonym(S): 1,3-Dihydro-3,3-dimethyl-1-(trifluoromethyl)-1,2-benziodoxole, Togni’s Reagent
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 250 MG | 696641-250-MG | In Stock | ₹ 10,705.93 |
| 1 G | 696641-1-G | In Stock | ₹ 35,018.88 |
| 5 G | 696641-5-G | In Stock | ₹ 58,942.13 |
696641 - 250 MG
In Stock
Quantity
1
Base Price: ₹ 10,705.93
GST (18%): ₹ 1,927.067
Total Price: ₹ 12,632.997
Quality Level
100
Assay
95%
form
powder
reaction suitability
reaction type: C-C Bond Formation
mp
75-79 °C
storage temp.
2-8°C
SMILES string
CC1(C)O[I](c2ccccc12)C(F)(F)F
InChI
1S/C10H10F3IO/c1-9(2)7-5-3-4-6-8(7)14(15-9)10(11,12)13/h3-6H,1-2H3
InChI key
HVAPLSNCVYXFDQ-UHFFFAOYSA-N
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | 1-Trifluoromethyl-3,3-Dimethyl-1,2-Benziodoxole | Aaron Chemicals LLC | ₹ 356.00 - ₹ 75,383.00 | |
 | 887144-97-0 | 3,3-Dimethyl-1-(trifluoromethyl)-1,2-benziodoxole | A2B Chem | ₹ 445.00 - ₹ 19,313.00 |
Related Products
Description
- Application: Easily accessible hypervalent iodine compound acting as an electrophilic CF3-transfer reagent for direct, mild, and efficient trifluoromethylation.[1] Trifluoromethylation of a variety of compounds including:Secondary and primary aryl- and alkylphospines[1] Phenols[2] Peptides containing cysteine residudes by SPPS and electrophilic S-trifluoromethylation[3] Arenes and N-heterocycles[4] Electrophilic N-trifluoromethylation of Arozoles[5]
SAFETY INFORMATION
Pictograms
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Flam. Sol. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Compare Similar Items
Show Difference
Quality Level: 100
Assay: 95%
form: powder
reaction suitability: reaction type: C-C Bond Formation
mp: 75-79 °C
storage temp.: 2-8°C
SMILES string: CC1(C)O[I](c2ccccc12)C(F)(F)F
InChI: 1S/C10H10F3IO/c1-9(2)7-5-3-4-6-8(7)14(15-9)10(11,12)13/h3-6H,1-2H3
InChI key: HVAPLSNCVYXFDQ-UHFFFAOYSA-N
Quality Level:
100
Assay:
95%
form:
powder
reaction suitability:
reaction type: C-C Bond Formation
mp:
75-79 °C
storage temp.:
2-8°C
SMILES string:
CC1(C)O[I](c2ccccc12)C(F)(F)F
InChI:
1S/C10H10F3IO/c1-9(2)7-5-3-4-6-8(7)14(15-9)10(11,12)13/h3-6H,1-2H3
InChI key:
HVAPLSNCVYXFDQ-UHFFFAOYSA-N
Quality Level: __
Assay: 98%
form: powder
reaction suitability: core: nickelreagent type: catalyst
mp: >300 °C
storage temp.: __
SMILES string: Cl[Ni]Cl.COCCOC
InChI: 1S/C4H10O2.2ClH.Ni/c1-5-3-4-6-2;;;/h3-4H2,1-2H3;2*1H;/q;;;+2/p-2
InChI key: OCMNCWNTDDVHFK-UHFFFAOYSA-L
Quality Level:
__
Assay:
98%
form:
powder
reaction suitability:
core: nickelreagent type: catalyst
mp:
>300 °C
storage temp.:
__
SMILES string:
Cl[Ni]Cl.COCCOC
InChI:
1S/C4H10O2.2ClH.Ni/c1-5-3-4-6-2;;;/h3-4H2,1-2H3;2*1H;/q;;;+2/p-2
InChI key:
OCMNCWNTDDVHFK-UHFFFAOYSA-L
Quality Level: 100
Assay: __
form: powder
reaction suitability: core: palladiumreaction type: Buchwald-Hartwig Cross Coupling Reactionreaction type: Cross Couplingsreaction type: Heck Reactionreaction type: Hiyama Couplingreaction type: Negishi Couplingreaction type: Sonogashira Couplingreaction type: Stille Couplingreaction type: Suzuki-Miyaura Couplingreagent type: catalyst
mp: __
storage temp.: __
SMILES string: Cl[Pd]Cl.C(CP(c1ccccc1)c2ccccc2)CP(c3ccccc3)c4ccccc4
InChI: 1S/C27H26P2.2ClH.Pd/c1-5-14-24(15-6-1)28(25-16-7-2-8-17-25)22-13-23-29(26-18-9-3-10-19-26)27-20-11-4-12-21-27;;;/h1-12,14-21H,13,22-23H2;2*1H;/q;;;+2/p-2
InChI key: LDFBXJODFADZBN-UHFFFAOYSA-L
Quality Level:
100
Assay:
__
form:
powder
reaction suitability:
core: palladiumreaction type: Buchwald-Hartwig Cross Coupling Reactionreaction type: Cross Couplingsreaction type: Heck Reactionreaction type: Hiyama Couplingreaction type: Negishi Couplingreaction type: Sonogashira Couplingreaction type: Stille Couplingreaction type: Suzuki-Miyaura Couplingreagent type: catalyst
mp:
__
storage temp.:
__
SMILES string:
Cl[Pd]Cl.C(CP(c1ccccc1)c2ccccc2)CP(c3ccccc3)c4ccccc4
InChI:
1S/C27H26P2.2ClH.Pd/c1-5-14-24(15-6-1)28(25-16-7-2-8-17-25)22-13-23-29(26-18-9-3-10-19-26)27-20-11-4-12-21-27;;;/h1-12,14-21H,13,22-23H2;2*1H;/q;;;+2/p-2
InChI key:
LDFBXJODFADZBN-UHFFFAOYSA-L
Quality Level: 100
Assay: ≥98.0% (HPLC)
form: __
reaction suitability: __
mp: 100-102 °C (lit.)
storage temp.: __
SMILES string: CN(C)c1ccc(cc1)C(c2ccccc2)c3ccc(cc3)N(C)C
InChI: 1S/C23H26N2/c1-24(2)21-14-10-19(11-15-21)23(18-8-6-5-7-9-18)20-12-16-22(17-13-20)25(3)4/h5-17,23H,1-4H3
InChI key: __
Quality Level:
100
Assay:
≥98.0% (HPLC)
form:
__
reaction suitability:
__
mp:
100-102 °C (lit.)
storage temp.:
__
SMILES string:
CN(C)c1ccc(cc1)C(c2ccccc2)c3ccc(cc3)N(C)C
InChI:
1S/C23H26N2/c1-24(2)21-14-10-19(11-15-21)23(18-8-6-5-7-9-18)20-12-16-22(17-13-20)25(3)4/h5-17,23H,1-4H3
InChI key:
__