1036588-32-5 Usage
General Description
4-Isopropoxy-3-methoxybenzyl chloride is a chemical compound with the molecular formula C11H15ClO2. It is a benzyl chloride derivative with an isopropoxy group and a methoxy group attached to the benzene ring. 4-Isopropoxy-3-methoxybenzyl chloride is a colorless liquid with a strong odor, and it is commonly used as a building block in the synthesis of organic compounds and pharmaceuticals. It is also utilized in the development of new materials and chemical processes. Additionally, 4-Isopropoxy-3-methoxybenzyl chloride has potential applications in the field of medicinal chemistry, specifically in the design and creation of new drugs and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 1036588-32-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,5,8 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1036588-32:
(9*1)+(8*0)+(7*3)+(6*6)+(5*5)+(4*8)+(3*8)+(2*3)+(1*2)=155
155 % 10 = 5
So 1036588-32-5 is a valid CAS Registry Number.
1036588-32-5Relevant articles and documents
Design and total synthesis of Mannich derivatives of marine natural product lamellarin D as cytotoxic agents
Shen, Li,Xie, Nan,Yang, Bo,Hu, Yongzhou,Zhang, Yongmin
, p. 807 - 817 (2014/10/15)
Enlightened by the modification route from Camptothecin (CPT) to Topotecan and based on classical drug design theory, a series of Mannich derivatives of lamellarin D were designed and synthesized in 26-27 steps starting from vanillin and isovanilin. All synthesized compounds were then biologically evaluated for their in vitro anti-cancer activities and Topo I inhibitory activities. The results showed that most target compounds exhibited Topo I inhibitory activities in equivalent level with that of lamellarin D. Compound SL-9 exhibited better Topo I inhibitory activity than that of lamellarin D. Compounds SL-2, SL-3, SL-4, SL-5 and SL-11 exhibited better anti-proliferative activity against HT-29 cells than that of lamellarin D.
