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The term "2-cyclopropyl-" refers to a chemical structure where a cyclopropyl group, which is a three-membered carbon ring, is attached to the 2nd position of a molecule. This specific arrangement can significantly influence the molecule's properties, such as its reactivity, stability, and physical characteristics. Cyclopropyl groups are known for their unique strain due to the bond angles being less than the ideal 109.5 degrees for sp3 hybridized carbon atoms, which can affect the molecule's electronic properties and reactivity. The presence of a 2-cyclopropyl group in a chemical compound can lead to distinct chemical behaviors and is often found in pharmaceuticals and other organic compounds where such strained ring systems are exploited for their unique properties.

6712-34-1

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6712-34-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6712-34-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,1 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6712-34:
(6*6)+(5*7)+(4*1)+(3*2)+(2*3)+(1*4)=91
91 % 10 = 1
So 6712-34-1 is a valid CAS Registry Number.

6712-34-1Downstream Products

6712-34-1Relevant academic research and scientific papers

Enantioselective total synthesis of vicenistatin, a novel 20-membered macrocyclic lactam antitumor antibiotic

Matsushima, Yoshitaka,Itoh, Hiroaki,Nakayama, Takuya,Horiuchi, Sayo,Eguchi, Tadashi,Kakinuma, Katsumi

, p. 949 - 958 (2007/10/03)

Enantioselective total synthesis of an antitumor antibiotic, vicenistatin, featuring a 20-membered macrocyclic lactam glycoside with the amino sugar vicenisamine, has been achieved. Key reactions in the synthesis of macrolactam aglycone involved Suzuki cross-coupling and Evans asymmetric aldol reaction. Penultimate glycosidation of the O-TMS-aglycone with appropriately protected 1-O-acetyl amino sugar and final deprotection allowed accomplishment of the total synthesis.

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