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(1S,2S,3S)-2-Formyl-3-methyl-α-methylenecyclopentaneacetaldehyde is a complex organic compound with a unique chiral structure. It is characterized by its cyclopentane ring, which is a five-membered carbon ring, and the presence of a formyl group (aldehyde) at the 2-position, a methyl group at the 3-position, and an α-methylene group. The α-methylene group refers to a carbon-carbon double bond adjacent to a carbonyl group, which in this case is part of the cyclopentane ring. The compound's stereochemistry is defined by the three chiral centers at the 1, 2, and 3 positions, all of which have the S configuration. This specific arrangement of atoms and functional groups gives the compound its distinct chemical properties and reactivity. It is important in organic chemistry for its potential applications in the synthesis of more complex molecules and as a building block in various chemical reactions.

3671-76-9

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3671-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3671-76-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,7 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3671-76:
(6*3)+(5*6)+(4*7)+(3*1)+(2*7)+(1*6)=99
99 % 10 = 9
So 3671-76-9 is a valid CAS Registry Number.

3671-76-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-anisomorphal

1.2 Other means of identification

Product number -
Other names (1S,2S,5S)-2-(1-Formyl-vinyl)-5-methyl-cyclopentanecarbaldehyde

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3671-76-9 SDS

3671-76-9Relevant academic research and scientific papers

Resolution and utilization of ethyl 5-hydroxycyclopent-1-enecarboxylate: Enantioselective synthesis of (+)-mitsugashiwalactone and (-)-dolichodial

Yamane,Takahashi,Ogasawara

, p. 444 - 448 (2007/10/02)

Optically pure ethyl 5-hydroxycyclopent-1-enecarboxylate has been obtained with its acetate in both enantiomeric forms in excellent optical yields from racemic ethyl 5-hydroxycyclopent-1-enecarboxylate by lipase-mediated kinetic resolution. The optically pure (R)-enantiomer thus obtained has been transformed into two naturally occurring iridoid monoterpenes, (+)-mitsugashiwalactone and (-)-dolichodial.

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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