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Methyl 15,16-dihydrosandaracopimarate is a chemical compound derived from the diterpenoid class, which are naturally occurring organic compounds found in plants. It is characterized by a molecular formula of C20H32O2 and a molecular weight of 304.47 g/mol. Methyl 15,16-dihydrosandaracopimarate is a dihydro derivative of sandaracopimaric acid, which is a component of the resin from the sandarac tree (Callitris spp.). Methyl 15,16-dihydrosandaracopimarate is synthesized by reducing the double bond between carbons 15 and 16 in the parent compound, resulting in a more stable and less reactive molecule. It is used in various applications, including the synthesis of other diterpenoid derivatives and as a potential intermediate in the production of pharmaceuticals and agrochemicals.

3867-54-7

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3867-54-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3867-54-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,6 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3867-54:
(6*3)+(5*8)+(4*6)+(3*7)+(2*5)+(1*4)=117
117 % 10 = 7
So 3867-54-7 is a valid CAS Registry Number.

3867-54-7Upstream product

3867-54-7Downstream Products

3867-54-7Relevant academic research and scientific papers

β-Stereospecific Hydroboration of 13-epi-Pimar-8(14)-enes

Feliciano, Arturo San,Medarde, Manuel,Caballero, Esther,Tome, Fernando,Hebrero, Belen

, p. 1665 - 1670 (2007/10/02)

β-Stereospecific hydroborations of the Δ8(14)-double bond in 13-epi-pimarenes were achieved in the absence of functional groups at C-16 or a double bond at C-15.The reaction carried out on 15,16-dihydrosandaracopimaric derivatives needed more time and a large excess of reagent due to stereochemical restrictions in the transition state.

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