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3-(1-nitrocyclohexyl)propanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76877-76-4

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76877-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76877-76-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,7 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76877-76:
(7*7)+(6*6)+(5*8)+(4*7)+(3*7)+(2*7)+(1*6)=194
194 % 10 = 4
So 76877-76-4 is a valid CAS Registry Number.

76877-76-4Relevant academic research and scientific papers

Synthesis of cyclic hydroxamic acids from aliphatic nitro compounds

Thomas, Achamma,Rajappa, Srinivasachari

, p. 10571 - 10580 (2007/10/02)

A novel method for the synthesis of five membered α-substituted cyclic hydroxamic acids from aliphatic nitro compounds including nitro acetic acid derivatives is described. Michael addition of allyl acrylate to these compounds followed by Pd(0) catalyzed

Synthesis and evaluation of (piperidinomethylene)bis(phosphonic acid) derivatives as anti-osteoporosis agents

Mimura,Hayashida,Nomiyama,Ikegami,Iida,Tamura,Hiyama,Ohishi

, p. 1971 - 1986 (2007/10/02)

Some (piperidinomethylene)bis(phosphonic acid) derivatives were prepared and their activity to inhibit a rise in serum calcium induced by parathyroid hormone in thyroparathyroidectomised rats was evaluated. Several (4- alkylidene-, 4,4-dialkyl-, or 4-alkyl-4- halopiperidinomethylene)bis(phosphonic acid) derivatives showed considerable inhibitory activity. But compounds having aromatic and polar substituents such as azido, hydroxy, amino and amido on the piperidine ring were generally inactive. In this study, two 4-alkylidene compounds (8a and 8b) and a 4,4- cyclic dialkyl compound (61) showed potent activity when administered either intravenously or perorally.

Producing substituted 2-cyclopentenones

-

, (2008/06/13)

A process is provided for producing substituted 2-cyclopentenones represented by the general formula: STR1 where R1, R2, R3, R4, and R5 are hydrogen or lower aliphatic hydrocarbyl groups. The process comprises treating a nitroalkane with a substituted acrylic acid ester in the presence of a base, followed by saponification, to yield a substituted 4-nitropentanoic acid which acid is then treated with strong acid under dehydrative conditions to yield the subject 2-cyclopentenone.

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