(S)-(+)-ALPHA-(TRIFLUOROMETHYL)BENZYL ALCOHOL

Product Name: (S)-(+)-ALPHA-(TRIFLUOROMETHYL)BENZYL ALCOHOL
CAS No.: 340-06-7
Chemical Name: (S)-(+)-ALPHA-(TRIFLUOROMETHYL)BENZYL ALCOHOL
Synonyms: (+)-PHENYL(TRIFLUOROMETHYL)CARBINOL;(1S)-1-Phenyl-2,2,2-trifluoroethanol;(S)-2,2,2-TRIFLUORO-1-PHENYL-ETHANOL;(1S)-2,2,2-Trifluoro-1-phenyl-ethanol;(S)-α-(Trifluoromethyl)benzenemethanol;(αS)-α-(Trifluoromethyl)benzenemethanol;(S)-(+)-1-PHENYL-2,2,2-TRIFLUOROETHANOL;(S)-(+)-2,2,2-TRIFLUORO-1-PHENYLETHANOL;(S)-(+)-α-(TRIFLUOROMETHYL)BENZYLALCOHOL;(s)-(+)-α-(trifluoromethyl)benzyl alcohol
CBNumber: CB4402563
Molecular Formula: C8H7F3O
Formula Weight: 176.14
MOL File: 340-06-7.mol

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(S)-(+)-ALPHA-(TRIFLUOROMETHYL)BENZYL ALCOHOL Property

Boiling point:: 73-76 °C9 mm Hg(lit.)
Density: 1.3 g/mL at 25 °C(lit.)
refractive index: n20/D 1.462(lit.)
Flash point:: 184 °F
storage temp.: Inert atmosphere,Room Temperature
form: Liquid
pka: 11.91±0.10(Predicted)
color: Clear colorless to pale yellow
optical activity: [α]20/D +31.3±0.5°, neat
BRN: 2327547
InChI: 1S/C8H7F3O/c9-8(10,11)7(12)6-4-2-1-3-5-6/h1-5,7,12H/t7-/m0/s1
InChIKey: VNOMEAQPOMDWSR-ZETCQYMHSA-N
SMILES: O[C@@H](c1ccccc1)C(F)(F)F

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Safety

Hazard Codes: Xi,C
Risk Statements: 36/37/38
Safety Statements: 26-36
RIDADR: NA 1993 / PGIII
WGK Germany: 3
F: 10-23
HS Code: 29062990
Storage Class: 10 - Combustible liquids
Hazard Classifications: Eye Irrit. 2
Skin Irrit. 2
STOT SE 3

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 411140
Product name: (S)-(+)-α-(Trifluoromethyl)benzyl alcohol
Purity: 99%
Packaging: 1g
Price: $869
Updated: 2025/07/31

TCI Chemical

Product number: P1368
Product name: (S)-(+)-alpha-(Trifluoromethyl)benzyl Alcohol
Purity: >98.0%(GC)
Packaging: 1g
Price: $237
Updated: 2025/07/31

TRC

Product number: T779065
Product name: (S)-(+)-α-(Trifluoromethyl)benzyl alcohol
Packaging: 50mg
Price: $70
Updated: 2021/12/16

Apolloscientific

Product number: PC0769
Product name: (1S)-(+)-1-Phenyl-2,2,2-trifluoroethan-1-ol
Purity: 99%
Packaging: 1g
Price: $95
Updated: 2021/12/16

AK Scientific

Product number: 4207AL
Product name: (S)-(+)-alpha-(Trifluoromethyl)benzyl Alcohol
Packaging: 100mg
Price: $98
Updated: 2021/12/16

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(S)-(+)-ALPHA-(TRIFLUOROMETHYL)BENZYL ALCOHOL Chemical Properties,Usage,Production

Uses

(S)?-?(+)?-?α-?(Trifluoromethyl)?benzyl Alcohol is used in the synthesis of metal-organic framework compounds which may have mesoporous properties.

Purification Methods

Purify the chiral alcohols by fractional distillation preferably in a vacuum. [Morrison & Ridgeway Tetrahedron Lett 573 1969, NMR: Pirkle & Beare J Am Chem Soc 90 6250 1968.] The racemate [340-05-6] has b 52-54o/2mm,57-59o/2mm, 64-65o/5mm, d 4 20 1.293, n D 20 1.457, and the 2-carbobenzoyl derivative has m 137-138o [Mosher et al. J Am Chem Soc 78 4374 1956]. [Beilstein 6 IV 3043.]

(S)-(+)-ALPHA-(TRIFLUOROMETHYL)BENZYL ALCOHOL Preparation Products And Raw materials

Raw materials

Preparation Products

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(S)-(+)-ALPHA-(TRIFLUOROMETHYL)BENZYL ALCOHOL Suppliers

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View Lastest Price from (S)-(+)-ALPHA-(TRIFLUOROMETHYL)BENZYL ALCOHOL manufacturers

Career Henan Chemical Co

Product: (S)-(+)-ALPHA-(TRIFLUOROMETHYL)BENZYL ALCOHOL 340-06-7
Price: US $5.50/KG
Min. Order: 1KG
Purity: 98%min
Supply Ability: 1kg,10kg,100kg
Release date: 2020-01-09

340-06-7, (S)-(+)-ALPHA-(TRIFLUOROMETHYL)BENZYL ALCOHOLRelated Search:

(R)-1-(3-BROMOPHENYL)ETHANOL (S)-(+)-2,2,2-TRIFLUORO-1-(9-ANTHRYL)ETHANOL 1,4-BIS(2-HYDROXYHEXAFLUOROISOPROPYL)BENZENE 1,3-BIS(2-HYDROXYHEXAFLUOROISOPROPYL)BENZENE (R)-(+)-alpha-Methoxy-alpha-trifluoromethylphenylacetic acid 1,1,1,3,3,3-HEXAFLUORO-2-PHENYL-2-PROPANOL 4-(2-HYDROXYHEXAFLUOROISOPROPYL)BENZOIC ACID (S)-(+)-ALPHA-(TRIFLUOROMETHYL)BENZYL ALCOHOL (S)-(+)-ALPHA-METHOXY-ALPHA-TRIFLUOROMETHYLPHENYLACETYL CHLORIDE HEXAFLUORO-2-(P-TOLYL)ISOPROPANOL 4-(HEXAFLUORO-2-HYDROXYISOPROPYL)ANILINE ALPHA-(TRIFLUOROMETHYL)BENZYL ALCOHOL ALPHA-(TRIFLUOROMETHYL)BENZYL ALCOHOL,ALPHA-(TRIFLUOROMETHYL)BENZYL ALCOHOL, 9 8% BIS(4-FLUOROPHENYL)TRIFLUOROMETHYL CARBINOL 4-CHLORO-(2-HYDROXYHEXAFLUOROISOPROPYL)BENZENE BIS[ALPHA,ALPHA-BIS(TRIFLUOROMETHYL)BENZENEMETHANOLATO]DIPHENYLSULFUR ALPHA-(TRIFLUOROMETHYL)BENZHYDROL 2-(2,5-Dimethylphenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol

(S)-(+)-2,2,2-TRIFLUORO-1-PHENYLETHANOL

(S)-2,2,2-TRIFLUORO-1-PHENYL-ETHANOL

(S)-(+)-1-PHENYL-2,2,2-TRIFLUOROETHANOL

(S)-(+)-ALPHA-(TRIFLUOROMETHYL)BENZYL ALCOHOL

(+)-PHENYL(TRIFLUOROMETHYL)CARBINOL

(S)-(+)-ALPHA-(TRIFLUOROMETHYL)BENZYL AL COHOL, 99% (97% EE/GLC)

(s)-(+)-α-(trifluoromethyl)benzyl alcohol

(+)-Phenyl(trifluoromethyl)carbinol, (S)-(+)-1-Phenyl-2,2,2-trifluoroethanol

(1S)-1-Phenyl-2,2,2-trifluoroethanol

(S)-α-(Trifluoromethyl)benzenemethanol

(αS)-α-(Trifluoromethyl)benzenemethanol

(1S)-(+)-1-Phenyl-2,2,2-trifluoroethan-1-ol

(S)-(+)-alpha-(Trifluoromethyl)benzyl alcohol 99%

(1S)-2,2,2-Trifluoro-1-phenyl-ethanol

(S)-2,2,2-Trifluoro-1-phenylethanol,99%e.e.

(1S)-(+)-1-Phenyl-2,2,2-trifluoroethan-1-ol 99%

(S)-(+)-α-(Trifluoromethyl)benzylAlcohol&gt

Benzenemethanol, α-(trifluoromethyl)-, (αS)-

(S)-(+)-α-(TRIFLUOROMETHYL)BENZYLALCOHOL

(alphaS)-alpha-(Trifluoromethyl)benzenemethanol

(S)-(+)-alpha-(Trifluoromethyl)benzyl alcohol, 99%,

(<i>S</i>)-(+)-α-(Trifluoromethyl)benzyl alcohol

(S)-(+)-α-(Trifluoromethyl)benzyl alcohol, CAS 340-06-7

340-06-7

Chiral Resolution Reagents

Chiral Resolving Reagents

Asymmetric Synthesis

Chiral

Alcohols, Hydroxy Esters and Derivatives

Chiral Compounds