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C10H13N3O5ClH, also known as [(2,3,4-Trihydroxyphenyl)methylene]hydrazide-serine Hydrochloride, is an impurity found in Benserazide (B120505). Benserazide is a drug that, when combined with the dopamine precursor Levodopa (D533751), is used in the management of Parkinson's disease. C10H13N3O5ClH consists of a hydrazide-serine structure with a hydrochloride ion attached, contributing to its chemical properties and potential applications.

1353749-74-2

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1353749-74-2 Usage

Uses

Used in Pharmaceutical Industry:
C10H13N3O5ClH is used as an impurity in the drug Benserazide, which is a crucial component in the treatment of Parkinson's disease. The compound plays a role in the effectiveness of the medication, as it is combined with Levodopa to manage the symptoms of the disease.
Used in Parkinson's Disease Management:
C10H13N3O5ClH is used as a component in the drug Benserazide for the management of Parkinson's disease. The combination of Benserazide and Levodopa helps to alleviate the symptoms of the disease by increasing the availability of dopamine in the brain, which is essential for proper motor function.

Check Digit Verification of cas no

The CAS Registry Mumber 1353749-74-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,3,7,4 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1353749-74:
(9*1)+(8*3)+(7*5)+(6*3)+(5*7)+(4*4)+(3*9)+(2*7)+(1*4)=182
182 % 10 = 2
So 1353749-74-2 is a valid CAS Registry Number.

1353749-74-2Downstream Products

1353749-74-2Relevant academic research and scientific papers

Synthesis method of benserazide hydrochloride

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Paragraph 0138- 0141, (2019/12/11)

The invention relates to a synthesis method of benserazide hydrochloride. According to the synthesis method, serine methyl ester hydrochloride is taken as the primary raw material, at first, amino protection reactions are carried out; and then amine-ester exchange reactions, condensation reactions, reduction reactions, and de-protection reactions are performed to obtain high purity benserazide hydrochloride. The synthesis method has the advantages that the raw materials are cheap and easily available, the operation is convenient, the product purity and yield of each step are high, and thus thesynthesis method is suitable for industrial production.

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