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p-(4-Hydroxyheptyl)-benzoesaeure is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56306-77-5

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56306-77-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56306-77-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,0 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56306-77:
(7*5)+(6*6)+(5*3)+(4*0)+(3*6)+(2*7)+(1*7)=125
125 % 10 = 5
So 56306-77-5 is a valid CAS Registry Number.

56306-77-5Upstream product

56306-77-5Downstream Products

56306-77-5Relevant academic research and scientific papers

The self-sufficient CYP102 family enzyme, Krac9955, from Ktedonobacter racemifer DSM44963 acts as an alkyl- and alkyloxy-benzoic acid hydroxylase

Maddigan, Natasha K.,Bell, Stephen G.

, p. 15 - 21 (2017)

A self-sufficient CYP102 family encoding gene (Krac_9955) has been identified from the bacterium Ktedonobacter racemifer DSM44963 which belongs to the Chloroflexi phylum. The characterisation of the substrate range of this enzyme was hampered by low levels of production using E. coli. The yield and purity of the Krac9555 enzyme was improved using a codon optimised gene, the introduction of a tag and modification of the purification protocol. The heme domain was isolated and in?vitro analysis of substrate binding and turnover was performed. Krac9955 was found to preferentially bind alkyl- and alkyloxy-benzoic acids (≥95% high spin, Kd?a self-sufficient CYP102 family member Krac9955 showed low levels of NAD(P)H oxidation activity for all the substrates tested though product formation was observed for many. For nearly all substrates the preferred site of hydroxylation of Krac9955 was eight carbons away from the carboxylate group with certain reactions proceeding at ≥ 90% selectivity. Krac9955 differs from CYP102A1 (P450Bm3), and is the first self-sufficient member of the CYP102 family of P450 enzymes which is not optimised for fast fatty acid hydroxylation close to the ω-terminus.

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