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(+/-)-Dolichol dial is a naturally occurring sesquiterpene, which is a type of organic compound derived from terpenes. It is characterized by its unique structure, featuring a 15-carbon backbone with a dialdehyde functional group. (+/-)-dolichodial is found in various plants and has been studied for its potential biological activities, including anti-inflammatory and cytotoxic effects. (+/-)-Dolichol dial has also been investigated for its role in the biosynthesis of dolichols, which are important for the formation of glycoproteins and glycolipids in cells. Due to its complex structure and potential applications, (+/-)-dolichol dial remains an interesting subject of research in the field of natural products chemistry and pharmacology.

1127-66-8

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1127-66-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1127-66-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1127-66:
(6*1)+(5*1)+(4*2)+(3*7)+(2*6)+(1*6)=58
58 % 10 = 8
So 1127-66-8 is a valid CAS Registry Number.

1127-66-8Relevant academic research and scientific papers

Pd(0) PROMOTED REARRANGEMENT OF 2-(1,3-BUTADIENYL)CYCLOPROPANE-1,1-DICARBOXYLATE ESTERS TO 2-ALKENYL-3-CYCLOPENTENE-1,1-DICARBOXYLATE ESTERS

Morizawa, Yoshitomi,Oshima, Koichiro,Nozaki, Hitosi

, p. 2871 - 2874 (2007/10/02)

The title dienylcyclopropanes smoothly rearrange to five-membered rings in the presence of Pd(0) catalyst under mild conditions.

SYNTHESE DU (+/-)-DOLICHODIAL TRANS-CIS

Beaupin, C.,Rossi, J. C.,Vidal, J. P.,Girard, J. P.,Passet, J.

, p. 1541 - 1542 (2007/10/02)

Key Word Index: Teucrium marum; Labiatae; trans-cis (+/-)-dolichodial; monoterpenoid; synthesis.

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