125873-65-6 Usage
General Description
[(1S)-2-methylidenecyclopropyl]acetic acid is a chemical compound with a complex structure that contains a cyclopropyl group and an acetic acid moiety. The presence of the cyclopropyl group, which is a three-membered ring containing one carbon-carbon double bond, gives the compound its unique structure and reactivity. The (1S) configuration indicates the stereochemistry of the molecule, specifying the arrangement of atoms around the chiral center. As an acetic acid derivative, it is likely to have similar properties to acetic acid, including acidity and potential reactivity in organic reactions. The presence of the methylidene group indicates a carbon with a double bond to a hydrogen and a single bond to another carbon, further contributing to the compound's structure and reactivity. Overall,[(1S)-2-methylidenecyclopropyl]acetic acid is a complex organic molecule with potential applications in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 125873-65-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,8,7 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 125873-65:
(8*1)+(7*2)+(6*5)+(5*8)+(4*7)+(3*3)+(2*6)+(1*5)=146
146 % 10 = 6
So 125873-65-6 is a valid CAS Registry Number.
125873-65-6Relevant articles and documents
Stereospecific inactivation of the general Acyl-CoA dehydrogenase from pig kidney by (R)-(-)-(methylenecyclopropyl)acetyl-CoA and (S)-(+)-(methylenecyclopropyl)acetyl-CoA
Baldwin, John E.,Ostrander, Robert L.,Simon, Clive D.,Widdison, Wayne C.
, p. 2021 - 2022 (1990)
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Enantioselective synthesis of the methylenecyclopropane derivative related to hypoglycine, from malic acid
Achmatowicz, Barbara,Kabat, Marek M.,Krajewski, Janusz,Wicha, Jerzy
, p. 10201 - 10210 (2007/10/02)
Synthesis of (S)-methylenecyclopropaneacetic acid starting from L-(-)-malic acid, via (2S)-O-tert-butyldimethylsilyl-1,2-epoxybutan-4-ol and 1-O-tert-butyldiphenylsilyl-5-benzenesulfonyl-6-trimethylsilylhexane-1,3-diols as the key intermediates, is descri
Mechanistic study on the inactivation of general Acyl-CoA dehydrogenase by a metabolite of hypoglycin A
Lai, Ming-Tain,Liu, Li-Da,Liu, Hung-Wen
, p. 7388 - 7397 (2007/10/02)
General acyl-CoA dehydrogenase (GAD) is a flavin-dependent (FAD) enzyme that catalyzes the oxidation of a fatty acyl-CoA to the corresponding α,β-enolyl-CoA. When GAD is exposed to (methylenecyclopropyl)acetyl-CoA (MCPA-CoA), a metabolite of hypoglycin A
