4-Bromophenylboronic Acid CAS 5467-74-3 Maʻemaʻe >99.5% (HPLC) Hale Hana Kiʻekiʻe

ʻO ka wehewehe pōkole:

Inoa Kemika: 4-Bromophenylboronic Acid

CAS: 5467-74-3

Maʻemaʻe: >99.5% (HPLC)

ʻAno: Keʻokeʻo a i ʻole-White Crystal Powder

ʻO ke kūlana kiʻekiʻe, ka hana kālepa

E-Mail: alvin@ruifuchem.com


Huahana Huahana

Nā Huahana Pili

Huahana Huahana

wehewehe:

Mea Manufacturer lako me High Quality, Commercial Production
Inoa Kemika: 4-Bromophenylboronic Acid CAS: 5467-74-3

Na Waiwai Kemika:

Inoa Kimia 4-Bromophenylboronic Acid
Nā huaʻōlelo like 4-Bromobenzeneboronic Acid
Helu CAS 5467-74-3
Helu CAT RF-PI1273
Kūlana Kūʻai I loko o ka waihona, hana unahi a hiki i 25 Tons/Mahina
ʻĀpana Molekala C6H6BBrO2
Kaumaha Molecular 200.83
Ka hoʻoheheʻe Hiki ke hoʻoheheʻe ʻia i ka Methanol;ʻAʻole hiki ke hoʻonā i ka wai
Brand Kemika Ruifu

Nā kikoʻī:

'ikamu Nā kikoʻī
Ka nana aku Keʻokeʻo a i ka pauka kristal keʻokeʻo
Maʻemaʻe / Kaʻina Hanana >99.5% (HPLC)
Lae hehee 284.0~288.0 ℃
Kaumaha kiko (25/25 ℃) 0.866~0.869
Nalo ma ka maloo <0.50%
Hoʻokahi haumia <0.30%
Huina paumaele <0.50%
Nā Metala Kaumaha (e like me Pb) <20ppm
Kūlana hoʻāʻo ʻOihana Kūlana
Hoʻohana Nā Kūwaena Lapaʻau;Nā Kūwaena OLED

Pūʻolo a me ka waiho ʻana:

Pūʻolo: ʻO ka ʻōmole, ʻeke ʻeke alumini, 25kg / pahu pahu pahu, a i ʻole e like me ka makemake o ka mea kūʻai aku.

Kūlana mālama:E mālama i loko o nā pahu i hoʻopaʻa ʻia ma kahi maloʻo a maloʻo;E pale i ka malamalama a me ka wai.

Pono:

1

FAQ:

Noi:

Hoʻohana nui ʻia ka 4-Bromophenylboronic Acid (CAS: 5467-74-3) ma ke ʻano he synthesis intermediates, pharmaceutical intermediates a me OLED intermediates, wai crystal intermediates a i ʻole mea hōʻike.ʻO ka 4-Bromophenylboronic Acid he mea hoʻohana no ka Palladium catalyzed Suzuki-Miyaura cross-couplings, Tandem-type Pd(II) -catalyzed oxidative Heck reaction a me intramolecular CH amidation sequence.Hoʻohana ʻia ia i ka hoʻomākaukau ʻana i nā modulators Protein a me nā enzymatic a me kinase inhibitors, Gallate-based obovatol analogs me ka hana anti-tumor.Hoʻohana ʻia ia ma ke ʻano he reagent no Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids me fluoroalkyl iodide, Pd-catalyzed arylative cyclization o alkyne-tethered enals a i ʻole enones ma o ka carbopalladation o nā alkynes, Copper-catalyzed cross-couplings.

E kākau i kāu leka ma aneʻi a hoʻouna mai iā mākou