Detail of > 1929-29-9
- CAS Number:
- 1929-29-9
- Name:
Benzenepropanoic acid,4-methoxy-
- Superlist Name:
- 3-(4-Methoxyphenyl)propionic acid
- Formula:
- C10H12O3
- Molecular Structure:

- Synonyms:
- Hydrocinnamicacid, p-methoxy- (6CI,7CI,8CI);3-(4-Methoxyphenyl)propanoic acid;3-(p-Methoxyphenyl)propanoic acid;3-[4-(Methyloxy)phenyl]propanoic acid;4-Methoxyhydrocinnamic acid;NSC 33134;NSC51509;p-Methoxyhydrocinnamic acid;b-(p-Methoxyphenyl)propionic acid;
- Molecular Weight:
- 180.20
- EINECS:
- 217-678-0
- Density:
- 1.144 g/cm3
- Melting Point:
- 98-100 °C(lit.)
- Boiling Point:
- 318.5 °C at 760 mmHg
- Flash Point:
- 125.8 °C
- Appearance:
- White tolight beige crystalline powder
- Hazard Symbols:
Xi- Risk Codes:
- 36/37/38
- Safety:
- 22-24/25-36-26Details
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Reference
- Chemical composition of Egyptian and UAE propolis
- All Rights Reserved. Chemical composition of Egyptian and UAE propolis. Said, Sobhi A.; Khan, Saeed A.; Ahmad, Iqbal; Ali, Hayam S. (Dubai Pharmacy College, Dubai, United Arab Emirates). Pakistan Journal of Pharmaceutical Sciences, 19(1), 58-61 (English) 2006 University of Karachi, Faculty of Pharmacy. CODEN: PJPSEN. ISSN: 1011-601X. DOCUMENT TYPE: Journal CA Section: 63 (Pharmaceuticals) The chem. compn. of propolis samples obtained from Behera, Egypt and Dubai, UAE, have been investigated by GC-MS and thirty four compds. have been tentatively identified. Some of these compds.Some commonly used reagents like 1592-38-7 and 1929-29-9 are used in this experiment. have not been reported previously in Egyptian propolis from different regions. The Egyptian sample contains a high amt. of aliph. (13.7%) and arom. (14.4%) acids. The alcs., phenols and esters account for about 17.0% of the total content analyzed. Some anthraquinone and flavone derivs. have also been detected (10%). The UAE sample is characterized by the presence of a high content of aliph. acids (15.2%) and a low content of arom. acids (4.3%). The aldehydes, alcs., phenols and esters amt. to about 9%. In addn. to these some other compds. (high mol. wt. alkanes, sugar derivs., anthraquinone derivs. and flavone derivs.) are also present to the extent of about 33%. .
- A rapid and efficient microwave-assisted synthesis of substituted 3-phenylpropionic acids from benzaldehydes in minutes
- Sharma, Anuj; Joshi, Bhupendra P.; Sinha, Arun K. (Natural Plant Products Division, Institute of Himalayan Bioresource Technology, Palampur 176061, India). Chemistry Letters, 32(12), 1186-1187 (English) 2003 Chemical Society of Japan. CODEN: CMLTAG. ISSN: 0366-7022. DOCUMENT TYPE: Journal CA Section: 25 (Benzene, Its Derivatives, and Condensed Benzenoid Compounds) A convenient, inexpensive, and efficient synthesis of 3-phenylpropionic acids by reacting benzaldehyde and malonic acid in acetic acid and piperidine into cinnamic acid in 77 to 89% followed by its redn. 104-88-1 and 1929-29-9 are cas registry numbers of chemicals which are used as reagents here. with PdCl2 in the diphase of formic acid and aq. sodium hydroxide is reported under microwave irradn. which utilizes short reaction time ranging 5 to 7 min to provide 3-phenylpropionic acids in moderate to high yield (69-86%) depending upon methoxy, methylenedioxy, and hydroxy groups present at the Ph ring. .
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