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Quinazoline, 4-methyl- (6CI,7CI,8CI,9CI)

Product Name
Quinazoline, 4-methyl- (6CI,7CI,8CI,9CI)
CAS No.
700-46-9
Chemical Name
Quinazoline, 4-methyl- (6CI,7CI,8CI,9CI)
Synonyms
4-Methylquinazoline;Quinazoline, 4-methyl-;Quinazoline, 4-methyl- (6CI,7CI,8CI,9CI)
CBNumber
CB51069773
Molecular Formula
C9H8N2
Formula Weight
144.17
MOL File
700-46-9.mol
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Quinazoline, 4-methyl- (6CI,7CI,8CI,9CI) Property

Melting point:
36-37 °C
Boiling point:
260 °C
Density 
1.141±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
2.69±0.30(Predicted)
Appearance
Light yellow to yellow Solid-Liquid Mixture
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

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

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

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

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

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

TRC
Product number
M321479
Product name
4-Methylquinazoline
Packaging
50mg
Price
$110
Updated
2021/12/16
TRC
Product number
M321479
Product name
4-Methylquinazoline
Packaging
10mg
Price
$45
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0362651
Product name
4-METHYLQUINAZOLINE
Purity
95.00%
Packaging
5MG
Price
$505.73
Updated
2021/12/16
Ambeed
Product number
A331983
Product name
4-Methylquinazoline
Purity
95%
Packaging
5g
Price
$609
Updated
2021/12/16
Chemenu
Product number
CM142684
Product name
4-methylquinazoline
Purity
95%
Packaging
5g
Price
$879
Updated
2021/12/16
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Quinazoline, 4-methyl- (6CI,7CI,8CI,9CI) Chemical Properties,Usage,Production

Uses

4-Methylquinazoline is an abdominal sex pheromone in Jewel wasp and other animals.

Synthesis Reference(s)

Journal of the American Chemical Society, 73, p. 5777, 1951 DOI: 10.1021/ja01156a085

Synthesis

50-00-0

2142-69-0

700-46-9

GENERAL METHODS: 2'-Bromoacetophenone (1a) (100.0 mg, 0.5 mmol), benzaldehyde (2a) (58.0 mg, 0.55 mmol), CuCl (5.0 mg, 0.05 mmol), 25% ammonia (0.5 mL), and NMP (0.5 mL) were sequentially added to a 25 mL thick-walled Pyrex screw-capped tube, which was sealed under an atmosphere of air sealed under air atmosphere. The reaction mixture was placed in an oil bath at 80°C and stirred for 12 hours. After the reaction was completed, it was cooled to room temperature and the crude product was extracted with EtOAc three times (3.0 mL each time). The organic phases were combined and concentrated under reduced pressure to remove the solvent. The residue was dissolved with CH2Cl2 (4.0 mL) and n-docosane (62.1 mg, 0.2 mmol) was added as an internal standard for GC analysis. After analyzing the reaction mixture by GC and GC-MS, the volatile solvent was removed under reduced pressure and the residue was purified by silica gel column chromatography [eluent: petroleum ether, followed by a mixed solvent of petroleum ether/ethyl acetate (100:1 to 50:1)] to afford 4-methyl-2-phenylquinazoline (3a) (69.6 mg, 0.32 mmol, 63% yield) as a white solid.GC analysis showed that the GC yield of 3a was 65%.

References

[1] Tetrahedron, 2012, vol. 68, # 46, p. 9364 - 9370

Quinazoline, 4-methyl- (6CI,7CI,8CI,9CI) Preparation Products And Raw materials

Raw materials

Preparation Products

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Quinazoline, 4-methyl- (6CI,7CI,8CI,9CI) Suppliers

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700-46-9, Quinazoline, 4-methyl- (6CI,7CI,8CI,9CI)Related Search:


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