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(R)-N-(1-phenylethyl)pentamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1375463-88-9

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1375463-88-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1375463-88-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,5,4,6 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1375463-88:
(9*1)+(8*3)+(7*7)+(6*5)+(5*4)+(4*6)+(3*3)+(2*8)+(1*8)=189
189 % 10 = 9
So 1375463-88-9 is a valid CAS Registry Number.

1375463-88-9Downstream Products

1375463-88-9Relevant academic research and scientific papers

Efficient dynamic kinetic resolution of arylamines with Pd/layered double-hydroxide-dodecyl sulfate anion for racemization

Xu, Gang,Dai, Xiaoting,Fu, Simin,Wu, Jianping,Yang, Lirong

, p. 397 - 402 (2014/01/06)

A novel and efficient racemization catalyst, Pd/layered double-hydroxide-dodecyl sulfate anion, was prepared and used in the dynamic kinetic resolution (DKR) of arylamines. The undesired enantiomer was completely racemized at 55 C, allowing the catalyst to be compatible with biocatalysts. DKR proceeded smoothly and showed a broad substrate scope, with good conversion and high product enantiomeric excesses (eep). The system could be reused more than 30 times without loss of conversion and eep value.

Self-disproportionation of enantiomers of non-racemic chiral amine derivatives through achiral chromatography

Nakamura, Tsuyoshi,Tateishi, Kaori,Tsukagoshi, Shiori,Hashimoto, Saori,Watanabe, Shotaro,Soloshonok, Vadim A.,Ace?a, José Luis,Kitagawa, Osamu

experimental part, p. 4013 - 4017 (2012/07/14)

Efficient self-disproportionation of enantiomers of several non-racemic chiral amines was achieved through conversion to N-acetamides and subsequent MPLC using an achiral column. The MPLC of these non-racemic N-acetamide derivatives gave the chart having a clear boundary between two fractions. Thus, in the less polar fraction, remarkable enantiomer enrichment was observed (>99%ee), while the ee of more polar fraction was considerably reduced. The magnitude of the enantiomer enrichments and depletions strongly depended on substituent on the amino group.

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