Cas:16817-32-6 3,5-dimethyl-1-benzofuran-2-carboxylate manufacturer & supplier

Chemical Name:3,5-dimethyl-1-benzofuran-2-carboxylate

CAS.NO:16817-32-6

Synonyms:3,5-dimethylbenzofuran-2-carboxylate;3,5-Dimethyl-benzofuran-2-carbonsaeure;3,5-dimethyl-benzofuran-2-carboxylic acid

Molecular Formula:C₁₁H₁₀O₃

Molecular Weight:190.19500

HS Code:2932999099

Physical and Chemical Properties:

Melting point:N/A

Boiling point:345.1ºC at 760mmHg

Density:1.256g/cm3

Index of Refraction:

PSA:50.44000

Exact Mass:190.06300

LogP:2.74780

Material Safety Information (Applicable for Hazard Chemicals)

RIDADR:

Packing Group:

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Related News: A week before Eli Lilly (LLY.N) disclosed to regulators that the U.S. Justice Department was investigating its New Jersey factory, the drugmaker told employees that its own inquiry, led by an outside law firm, found no evidence of wrongdoing there, according to a company memo reviewed by Reuters. 3,5-dimethyl-1-benzofuran-2-carboxylate manufacturer China has previously dealt with several bird flu outbreaks, the most recent in April 2019. In the new case, the H5N1 bird flu virus was found at a farm in the city of Shaoyang. The farm had 7,850 chickens, and more than half have died from the bird flu, the ministry said. It called the strain ��highly pathogenic.�� 3,5-dimethyl-1-benzofuran-2-carboxylate supplier China has previously dealt with several bird flu outbreaks, the most recent in April 2019. In the new case, the H5N1 bird flu virus was found at a farm in the city of Shaoyang. The farm had 7,850 chickens, and more than half have died from the bird flu, the ministry said. It called the strain ��highly pathogenic.�� 3,5-dimethyl-1-benzofuran-2-carboxylate vendor Without disclosing or confirming the number of vaccine doses, the FDA said in a news release that it had authorized two batches of the vaccine for use, that several other batches were not suitable for use and that others were being evaluated. 3,5-dimethyl-1-benzofuran-2-carboxylate factory Pre-approval Access Programs (also known as expanded access, early access, compassionate use, named patient supply) are regulatory-compliant processes permitting experimental agents in development to be made available upon the request of a physician or a patient for appropriate patients for whom no alternative treatment option exists in their country.