2460-87-9 Usage
General Description
4-Tert-Butoxyphenol, also known as 4-(tert-Butoxy)phenol, is a chemical compound commonly used as a stabilizer and antioxidant in the production of polymers and plastics. It is a phenolic compound with a molecular formula of C10H14O2, and is a clear, colorless, and viscous liquid at room temperature. 4-Tert-Butoxyphenol is also utilized as an intermediate in the production of pharmaceuticals and other chemicals, and as a fragrance ingredient in various personal care products. It is known for its ability to inhibit the degradation of polymers caused by heat, light, and oxidation, making it an important additive in the manufacturing of plastic products and materials. Additionally, 4-Tert-Butoxyphenol is considered to be relatively low in toxicity and safe for human and environmental use when handled and stored properly.
Check Digit Verification of cas no
The CAS Registry Mumber 2460-87-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,6 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2460-87:
(6*2)+(5*4)+(4*6)+(3*0)+(2*8)+(1*7)=79
79 % 10 = 9
So 2460-87-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O2/c1-10(2,3)12-9-6-4-8(11)5-7-9/h4-7,11H,1-3H3
2460-87-9Relevant articles and documents
Copper-Catalyzed Hydroxylation of (Hetero)aryl Halides under Mild Conditions
Xia, Shanghua,Gan, Lu,Wang, Kailiang,Li, Zheng,Ma, Dawei
supporting information, p. 13493 - 13496 (2016/10/31)
The combination of Cu(acac)2 and N,N′-bis(4-hydroxyl-2,6-dimethylphenyl)oxalamide (BHMPO) provides a powerful catalytic system for hydroxylation of (hetero)aryl halides. A wide range of (hetero)aryl chlorides bearing either electron-donating or -withdrawing groups proceeded well at 130 °C, delivering the corresponding phenols and hydroxylated heteroarenes in good to excellent yields. When more reactive (hetero)aryl bromides and iodides were employed, the hydroxylation reactions completed at relatively low temperatures (80 and 60 °C, respectively) at low catalytic loadings (0.5 mol % Cu).
Angiotensin II antagonists
-
, (2008/06/13)
This invention provides novel heterocyclic derivatives, their pharmaceutical formulations, and their use for antagonizing angiotensin II receptors in mammals.
Angiotensin II antagonists
-
, (2008/06/13)
This invention provides novel phenyl and heterocyclic derivatives, their pharmaceutical formulations and their methods of use for antagonizing angiotensin II receptors in mammals.
