127087-62-1 Usage
General Description
Tert-butyl 3-hydroxy-2-phenylpropylcarbamate is a chemical compound that is often used as a UV filter in sunscreens and other personal care products. It is part of a group of chemicals known as organic carbamates, which are known for their ability to absorb and block harmful UV radiation. Tert-butyl 3-hydroxy-2-phenylpropylcarbamate is a white powder that is soluble in organic solvents and has a melting point of around 110°C. It is considered to be safe for use in cosmetics and personal care products, as it is not known to cause skin irritation or sensitization. Additionally, it is important to note that the use of this chemical compound is regulated by various government agencies to ensure its safe use in consumer products.
Check Digit Verification of cas no
The CAS Registry Mumber 127087-62-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,0,8 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 127087-62:
(8*1)+(7*2)+(6*7)+(5*0)+(4*8)+(3*7)+(2*6)+(1*2)=131
131 % 10 = 1
So 127087-62-1 is a valid CAS Registry Number.
127087-62-1Relevant articles and documents
Copper-catalyzed borylative aminomethylation of C-C double and triple bonds withN,O-acetal
Qiu, Xianfan,Xu, Liugen,Wang, Shuxia,Dai, Ying,Feng, Yunqiu,Gong, Chang,Tao, Chuanzhou
, p. 3279 - 3282 (2021)
A copper-catalyzed borylaminomethylation of multiple carbon-carbon bonds withN,O-acetal and bis(pinacolato)diboron has been disclosed that offers efficient and expedient access to γ-amino boronates. The products contain a valuable amine and boronate, whic
First synthesis of the antifungal and antibacterial agent cladobotryal
Clive, Derrick L. J.,Huang, Xiaojun
, p. 2062 - 2063 (2007/10/03)
The antifungal and antibacterial agent cladobotryal (1) was synthesized by a convergent route from lactone 5 and aldehyde 12, a key step in the elaboration of the pyridinone ring being conversion of a t-BuOC(O) group on nitrogen into an i-Pr3SiOC(O) group.
