CAS 619-41-0|2-bromo-4'-methylacetophenone

Introduction：Basic information about CAS 619-41-0|2-bromo-4'-methylacetophenone, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Table of Contents

1. Names
2. Chemical & Physical Properties
3. Safety Information
4. Customs
5. Articles2
6. Synonyms

Common Name	2-bromo-4'-methylacetophenone
CAS Number	619-41-0	Molecular Weight	213.071
Density	1.4±0.1 g/cm3	Boiling Point	263.6±15.0 °C at 760 mmHg
Molecular Formula	C₉H₉BrO	Melting Point	45-49 °C(lit.)
MSDS	USA	Flash Point	74.4±7.7 °C
Symbol	GHS07	Signal Word	Warning

Names

Name	2-Bromo-4'-methylacetophenone
Synonym	More Synonyms

Chemical & Physical Properties

Density	1.4±0.1 g/cm3
Boiling Point	263.6±15.0 °C at 760 mmHg
Melting Point	45-49 °C(lit.)
Molecular Formula	C₉H₉BrO
Molecular Weight	213.071
Flash Point	74.4±7.7 °C
Exact Mass	211.983673
PSA	17.07000
LogP	2.65
Vapour Pressure	0.0±0.5 mmHg at 25°C
Index of Refraction	1.563
InChIKey	KRVGXFREOJHJAX-UHFFFAOYSA-N
SMILES	Cc1ccc(C(=O)CBr)cc1
Storage condition	-20?C Freezer, Under Inert Atmosphere
Stability	Stable. Incompatible with strong oxidizing agents, strong bases.

Safety Information

Symbol	GHS07
Signal Word	Warning
Hazard Statements	H315-H319-H335
Precautionary Statements	P261-P305 + P351 + P338
Personal Protective Equipment	dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes	Xi:Irritant;
Risk Phrases	R36/37/38
Safety Phrases	S26-S27-S37/39
RIDADR	UN 2811
WGK Germany	3
Hazard Class	6.1
HS Code	2914700090

Customs

HS Code	2914700090
Summary	HS: 2914700090 halogenated, sulphonated, nitrated or nitrosated derivatives of ketones and quinones, whether or not with other oxygen function Tax rebate rate:9.0% Supervision conditions:none VAT:17.0% MFN tariff:5.5% General tariff:30.0%

Articles2

Efficient solid-phase synthesis of 2-substituted-3-hydroxy-4(1H)-quinolinone-7-carboxamides with two diversity positions.

J. Comb. Chem. 9(5) , 793-6, (2007)

A highly efficient solid-phase synthesis of 2-substituted-3-hydroxy-4(1H)-quinolinone-7-carboxamides was developed using anthranilates and bromoketones as the key synthons. Primary amines immobilized ...

Use of fluorous silica gel to separate fluorous thiol quenching derivatives in solution-phase parallel synthesis Zhang W, et al.

Tetrahedron 58(20) , 3871-75, (2002)

Synonyms

Ethanone, 2-bromo-1-(4-methylphenyl)-

2-bromo-4'-methylacetophenone

EINECS 226-267-5

2-Bromo-1-(4-methylphenyl)ethanone

MFCD00009312

Acetophenone, 2-bromo-4'-methyl-

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