Basic information
- CAS
127852-28-2- Standard SMILES
C[C@@H](O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1- InChIKey
MMSCIQKQJVBPIR-RXMQYKEDSA-N- Molecular formula
- C10H8F6O
- Average molar mass
- 258.16 g/mol
- Monoisotopic mass
- 258.04793385
Names & identifiers
- Preferred name
- (alphaR)-alpha-Methyl-3,5-bis(trifluoromethyl)benzenemethanol
- IUPAC
- (1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethanol
- English name
- (R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol
- Molecular formula
- C10H8F6O
- Molecular weight
- 258.16
Names & synonyms
Show more names
Database identifiers
- CAS
127852-28-2- PubChem CID
- 2779031
- DTXSID
DTXSID80381243- UNII
- 26EP435WQ9
- EC Number
- 603-245-7
- Nikkaji
- J1.427.078G
Properties
Computed structural properties
- XLogP
- 3.2
- Topological polar surface area
- 20.2 Ų
- Hydrogen bond donors
- 1
- Hydrogen bond acceptors
- 7
- Rotatable bonds
- 1
- Heavy atoms
- 17
- Formal charge
- 0
- Complexity
- 237
Physicochemical properties
- Melting point
- 53 · 53-58℃
- Boiling point
- 175.8 · 175.8±35.0 °C(Predicted)
- Density
- 1.376 · 1.376±0.06 g/cm3(Predicted)
- storage temp.
- -20 °C · -20°C Freezer
- solubility
- Acetonitrile (Slightly), Chloroform (Slightly)
- pka
- 13.99 · 13.99±0.20(Predicted)
- form
- Powder
- color
- White
- optical activity
- 27 · [α]/D +27±1°, c = 1 in acetonitrile
- λmax
- 272 nm · 272nm(MeOH)(lit.)
- InChI
- InChI=1/C10H8F6O/c1-5(17)6-2-7(9(11,12)13)4-8(3-6)10(14,15)16/h2-5,17H,1H3/t5-/s3
- InChIKey
- MMSCIQKQJVBPIR-RXMQYKEDSA-N
- SMILES
- C(C1C=C([C@H](O)C)C=C(C(F)(F)F)C=1)(F)(F)F |&1:4,r|
- CAS DataBase Reference
- 127852 · 127852-28-2(CAS DataBase Reference)
- FDA UNII
- 26 EP435WQ9 · 26EP435WQ9
- UNSPSC Code
- 12352002 · 12352002
- Symbol(GHS)
- 7 · GHS07
- Signal word
- Warning
- Hazard statements
- 315 · H315-H319-H302-H335
- Precautionary statements
- 261 · P261-P280a-P304+P340-P305+P351+P338-P405-P501a-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
- PPE
- 95 · dust mask type N95 (US), Eyeshields, Gloves
- Hazard Codes
- Xi,Xn
- Risk Statements
- 36 · 36/37/38-52/53-22
- Safety Statements
- 26 · 26-36/37/39-61
- WGK Germany
- 3 · 3
- Hazard Note
- Irritant
- HS Code
- 29062990 · 29062990
- Storage Class
- 11 · 11 - Combustible Solids
- Hazard Classifications
- 4 Oral · Acute Tox. 4 Oral
Safety & regulation
GHS classification
GHS Classification
Warning
H302 (95.5%): Harmful if swallowed [Warning Acute toxicity, oral]
P264, P270, P301+P317, P330, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 44 reports by companies from 3 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
Safety data
- PPE
- dust mask type N95 (US), Eyeshields, Gloves
- wgk
- 3
- hs_code
- 29062990
- risk_code
- 36/37/38-52/53-22
- Signal word
- Warning
- Symbol(GHS)
- GHS07
- hazard_code
- Xi,Xn
- hazard_note
- Irritant
- safety_code
- 26-36/37/39-61
- Storage Class
- 11 - Combustible Solids
- Hazard statements
- H315-H319-H302-H335
- Hazard Classifications
- Acute Tox. 4 Oral
- Precautionary statements
- P261-P280a-P304+P340-P305+P351+P338-P405-P501a-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Chemistry & industry
Applications
Uses(R)-[3,5-bis (trifluoromethyl) phenyl] ethanol is an important chiral intermediate for the synthesis of novel chemotherapeutic and antiemetic drugs NK-1 receptor antagonists. Antidepressants have good potential efficacy in treating a range of central and peripheral nervous system depressions.
Uses(R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol is an intermediate in the synthesis of Aprepitant (A729800), a novel selective neurokinin-1 (NK-1) receptor antagonist. In vitro studies using human liver microsomes indicate that Aprepitant is metabolised primarily by CYP3A4 with minor metabolism by CYP1A2 and CYP2C19, and no metabolism by CYP2D6, CYP2C9, or CYP2E1. Antiemetic.
General Description(R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol is a key intermediate for the synthesis of aprepitant, a potent human neurokinin-1 (NK-1) receptor.
Preparation methods
PreparationAt present, the methods for preparing optically pure (R)-[3,5-bis (trifluoromethyl) phenyl] ethanol include chemical methods and biological methods. Chemical synthesis requires the use of expensive transition metal Ru and other chemical catalysts, complicated steps, harsh reaction conditions, high energy consumption, large pollution, and low yield. Biological law is the use of free enzymes or whole cells for catalytic preparation. It has the characteristics of mild reaction conditions, high catalytic efficiency, and strong specificity.
Upstream & downstream products
Upstream raw materials
Suppliers100 total
Related reactions
Compound notes
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