(S)-(+)-Mosher's acid chloride

Modify Date: 2024-01-02 23:00:40

(S)-(+)-Mosher's acid chloride structure	Common Name	(S)-(+)-Mosher's acid chloride
	CAS Number	39637-99-5	Molecular Weight	252.617
	Density	1.3±0.1 g/cm3	Boiling Point	213.5±0.0 °C at 760 mmHg
	Molecular Formula	C₁₀H₈ClF₃O₂	Melting Point	N/A
	MSDS	Chinese USA	Flash Point	90.0±0.0 °C
	Symbol	GHS05	Signal Word	Danger

Name	(R)-(-)-alpha-Methoxy-alpha-(trifluoromethyl)phenylacetyl chloride
Synonym	More Synonyms

Density	1.3±0.1 g/cm3
Boiling Point	213.5±0.0 °C at 760 mmHg
Molecular Formula	C₁₀H₈ClF₃O₂
Molecular Weight	252.617
Flash Point	90.0±0.0 °C
Exact Mass	252.016495
PSA	26.30000
LogP	5.03
Vapour Pressure	0.2±0.4 mmHg at 25°C
Index of Refraction	1.464
Storage condition	−20°C

(S)-(+)-Mosher's acid chloride MSDS(Chinese)

Symbol	GHS05
Signal Word	Danger
Hazard Statements	H314
Precautionary Statements	P280-P305 + P351 + P338-P310
Personal Protective Equipment	Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard Codes	C
Risk Phrases	34
Safety Phrases	26-27-36/37/39-45
RIDADR	UN 3265 8/PG 2
WGK Germany	3
Packaging Group	II
Hazard Class	8.0
HS Code	2918990090

HS Code	2918990090
Summary	2918990090. other carboxylic acids with additional oxygen function and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

High-performance liquid chromatographic resolution of enantiomers of 1-phenyl-2-aminopropanes (amphetamines) with four chiral reagents.

J. Chromatogr. A. 307 , 335, (1984)

High-performance liquid chromatography (HPLC) was employed for resolution of enantiomers of chiral ring-substituted 1-phenyl-2- aminopropanes (amphetamines) and 1-phenylethylamine following derivatiza...

Mosher ester analysis for the determination of absolute configuration of stereogenic (chiral) carbinol carbons.

Nat. Protoc. 2 , 2451-2458, (2007)

This protocol details the most commonly used nuclear magnetic resonance (NMR)-based method for deducing the configuration of otherwise unknown stereogenic, secondary carbinol (alcohol) centers (R1R2CH...

J.A. Dale, H.S. Mosher

J. Am. Chem. Soc. 95 , 512, (1973)

(-)-Mosher's Acid Chloride

(-)-α-Methoxy-α-(trifluoroMethyl)phenylacetyl Chloride

MFCD00067105

(S)-(+)-MTPA-Cl

Benzeneacetyl chloride, α-methoxy-α-(trifluoromethyl)-, (αS)-

Mosher's acid chloride

(R)-(-)-α-Methoxy-α-(trifluoromethyl)phenylacetyl chloride

(2S)-3,3,3-Trifluoro-2-methoxy-2-phenylpropanoyl chloride

(S)-Mosher's acid chloride

(-)-MTPA-Cl