(alphaR)-alpha-Methyl-3,5-bis(trifluoromethyl)benzenemethanol

HCID 2779031

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

(alphaR)-alpha-Methyl-3,5-bis(trifluoromethyl)benzenemethanolRefChem:405717127852-28-2(R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol(r)-1-(3,5-bis(trifluoromethyl)phenyl)ethanol(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethanolMFCD03093010(r)-1-[3,5-bis(trifluoromethyl)phenyl]ethan-1-ol(R)-1-(3,5-Bis-trifluoromethyl-phenyl)-ethanolC10H8F6OAprepitant Impurity 37(r)-1-(3,5-bis(trifluoromethyl)phenyl)ethan-1-ol
Show more names
C1oHgF6OR-MBT-PEL(R)-1-[3,5-Bis(trifLAprepitant Impurity 49Phenol,5-iodo-4-methyl-Fosaprepitant Impurity 25Rolapitant Intermediate 3Thiazole,2-bromo-9-methyl-(R)-1-[3,5- Bis(trifluoromethyl)phenyl]et
(1R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethan-1-olBenzenemethanol, alpha-methyl-3,5-bis(trifluoromethyl)-, (alphaR)-DTXSID8038124326EP435WQ9CS-D0702AKOS005063416(r)-[3,5-bis(trifluoromethyl)phenyl] ethanol(R)-1-[3,5-BIS(TRIFLUOROMETHYL)PHENYL)ETHANOL

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

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)

Safety & regulation

GHS classification

GHS Classification · 5 items

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

Hazard Classes and CategoriesAcute Tox. 4 (95.5%)

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

Chemistry & industry

Applications · 3 items

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 · 1 item

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.

Suppliers100 total

梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
上海恩氟佳科技有限公司15800445152 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
韶远科技(上海)有限公司021-50795510 4000665055 · [email protected]
中山奕安泰医药科技有限公司760-85282375 15900088539 · [email protected]

Related reactions

10 records

Compound notes

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