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Methyl-3-benzyloxy-2-methoxy-benzoat, also known as 3-benzyloxy-2-methoxybenzoic acid methyl ester, is a chemical compound with the molecular formula C16H16O5. It is a white crystalline solid that is soluble in organic solvents. Methyl-3-benzyloxy-2-methoxy-benzoat is characterized by the presence of a benzoic acid core, with a methyl group attached to the carboxylic acid, a benzyloxy group at the 3-position, and a methoxy group at the 2-position. It is often used as an intermediate in the synthesis of various pharmaceuticals and other organic compounds due to its versatile functional groups, which can be further modified in chemical reactions.

2169-24-6

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2169-24-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2169-24-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,6 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2169-24:
(6*2)+(5*1)+(4*6)+(3*9)+(2*2)+(1*4)=76
76 % 10 = 6
So 2169-24-6 is a valid CAS Registry Number.

2169-24-6Relevant academic research and scientific papers

POLYCYCLIC AMIDES AS UBE2K MODULATORS FOR TREATING CANCER

-

, (2021/07/10)

Provided are compounds of Formula (I) and pharmaceutically acceptable salts and compositions thereof, which are useful for treating conditions associated with modulation of UBE2K.

An Efficient Synthesis of the Naphthalene Subunits of the Protein Kinase C Inhibitor Calphostin C

Coleman, Robert S.,Grant, Eugene B.

, p. 1357 - 1359 (2007/10/02)

An efficient synthesis of bromonaphthalenes 5b-c, which represent suitably functionalized precursors to the perylenequinone ring system characteristic of the protein kinase C inhibitor calphostin C (1), is described and was based on the Diels-Alder reaction of o-quinol acetate 7 with 1,1,3-trioxygenated butadienes 6a-c, followed by selective, acid-promoted elimination of R3SiOH and AcOH to directly afford naphthalenes 11a-c.

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