Cas:196815-75-5 Bromobis(indenyl)vanadium manufacturer & supplier

We serve Chemical Name:Bromobis(indenyl)vanadium CAS:196815-75-5 to global customers since 2007, Pls send inquiry to info@nbinno.com or visit www.nbinno.com our official website should you have any interests. This site is for information only.

Bromobis(indenyl)vanadium

Chemical Name:Bromobis(indenyl)vanadium
CAS.NO:196815-75-5
Synonyms:Bromobis(indenyl)vanadium
Molecular Formula:C18H14BrV
Molecular Weight:361.15
HS Code:

Physical and Chemical Properties:
Melting point:N/A
Boiling point:N/A
Density:N/A
Index of Refraction:
PSA:
Exact Mass:
LogP:

Material Safety Information (Applicable for Hazard Chemicals)
RIDADR:
Packing Group:


Contact us for information like Bromobis(indenyl)vanadium chemical properties,Structure,melting point,boiling point,density,molecular formula,molecular weight,Bromobis(indenyl)vanadium physical properties,toxicity information,customs codes,safety, risk, hazard and MSDS, CAS,cas number,Bromobis(indenyl)vanadium Use and application,Bromobis(indenyl)vanadium technical grade,usp/ep/jp grade.


Related News: Australia’s ban followed an earlier move by the US Friday to deny entry to foreign nationals who have traveled in China in the last 14 days. Bromobis(indenyl)vanadium manufacturer Compared to white women, Black women are more likely to be diagnosed with breast cancer before age 50 or with estrogen receptor (ER)-negative and triple-negative breast cancer. Bromobis(indenyl)vanadium supplier The Branchburg factory first came under FDA scrutiny in late 2019, when agency inspectors began to document numerous quality control problems. By March, 2020, the FDA had deemed the manufacturing issues as “Official Action Indicated,” its most serious category of violation. Bromobis(indenyl)vanadium vendor Standard respiratory support therapies are used to treat the symptoms and wait for the virus to be cleared by itself. Bromobis(indenyl)vanadium factory The Branchburg factory first came under FDA scrutiny in late 2019, when agency inspectors began to document numerous quality control problems. By March, 2020, the FDA had deemed the manufacturing issues as “Official Action Indicated,” its most serious category of violation.