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(+/-)-Dolichol dial is a naturally occurring sesquiterpene, which is a type of organic compound derived from isoprene units. It is a key component in the biosynthesis of dolichols, a class of polyprenols that play a crucial role in various cellular processes, including protein glycosylation and the formation of the cell wall in yeast. Dolichol dial is characterized by its unique structure, featuring a dialdehyde functional group and a long, unsaturated hydrocarbon chain. Due to its importance in cellular metabolism, (+/-)-dolichol dial has been the subject of research in the fields of biochemistry and pharmacology, with potential applications in the development of therapeutic agents targeting diseases related to protein glycosylation abnormalities.

1198-22-7

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1198-22-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1198-22-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1198-22:
(6*1)+(5*1)+(4*9)+(3*8)+(2*2)+(1*2)=77
77 % 10 = 7
So 1198-22-7 is a valid CAS Registry Number.

1198-22-7Relevant academic research and scientific papers

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

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

, p. 1541 - 1542 (1980)

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

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.

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