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17795-24-3

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17795-24-3 Usage

General Description

The chemical 3-(propylsulphinyl)-L-alanine is a compound that belongs to the class of sulfoxides, which are organic compounds containing a sulfur atom bonded to two carbon atoms. It is derived from L-alanine, which is an amino acid that is important for protein synthesis and is found in many foods. The presence of the propylsulphinyl group in the compound gives it unique properties and potential biological activities. Sulfoxides have been studied for their potential therapeutic effects, including anti-inflammatory and antioxidant properties. 3-(propylsulphinyl)-L-alanine may have potential applications in the pharmaceutical and biotechnology industries for the development of new drugs and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 17795-24-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,7,9 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17795-24:
(7*1)+(6*7)+(5*7)+(4*9)+(3*5)+(2*2)+(1*4)=143
143 % 10 = 3
So 17795-24-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO3S/c1-2-3-11(10)4-5(7)6(8)9/h5H,2-4,7H2,1H3,(H,8,9)

17795-24-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-amino-3-propylsulfinylpropanoic acid

1.2 Other means of identification

Product number -
Other names Propiin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:17795-24-3 SDS

17795-24-3Downstream Products

17795-24-3Relevant articles and documents

A step-by-step crystallization for preparing thio alkyl/alkenyl cysteine sulfoxide method

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Paragraph 0061; 0062, (2017/05/26)

The invention discloses a method for preparing thioalkyl/alkenyl cysteine sulfoxide by fractional crystallization, belonging to the technical field of compound preparation. The method comprises the following steps: adding cysteine or cysteine salts, a sodium hydroxide solution and an R group (alkyl or alkenyl)-derived material into absolute ethanol in sequence for reaction to synthesize coarse ACSs, re-crystallizing ACSs, purifying, oxidizing to form ACSOs, and fractionally crystallizing to obtain natural dextrorotatory ACSOs, wherein the R group-derived material is replaced to synthesize different types of ACSOs in allium; enantiomers in racemes are separated by adopting the fractional crystallization method to obtain natural dextrorotatory ACSOs with optical activity. Compared with a conventional extraction method, the method has the characteristics that the yield and the purity are high, a conventional complicated extraction process is avoided, the product has the optical activity, and the physical property is close to that of natural extract; the product is used in the fields of health products, pharmaceuticals and the like, the effects of resisting bacteria and cancers, reducing blood fat and the like of ACSOs are brought into play, or the product serves as an intermediate such as an active ingredient-diallyl thiosulfinate for synthesizing allium.

Differential inhibition of human platelet aggregation by selected Allium thiosulfinates

Briggs, William H.,Xiao, Hang,Parkin, Kirk L.,Shen, Cunxi,Goldman, Irwin L.

, p. 5731 - 5735 (2007/10/03)

Thiosulfinates (TSs) have been implicated as a principle source of the antiplatelet property of raw onion and garlic juice. The in vitro responses of human platelets to dosages of four TSs were measured using whole blood aggregometry and compared by regression analysis. Of the compounds evaluated, methyl methane-TS (MMTS), propyl propane-TS (PPTS), and 2-propenyl 2-propene-TS (allicin) are present in freshly cut Allium vegetables, whereas ethyl ethane-TS (EETS) has not been detected. All TSs were synthesized using a model reaction system. PPTS and allicin had the strongest antiplatelet activity at 0.4 mM, inhibiting aggregation by 90 and 89%, respectively. At the same concentration, EETS and MMTS were significantly weaker, inhibiting 74 and 26%, respectively. Combinations of TSs were not additive in their inhibition of aggregation, indicating that the antiplatelet potential of Allium extracts cannot be easily predicted by quantifying organosulfur components. EETS, PPTS, and allicin were significantly more potent platelet inhibitors than aspirin at nearly equivalent concentrations.

On determination of the value of garlic preparations. 1. Chromatographic studies on the genuine contents of Allium sativum L.

Hoerhammer,Wagner,Seitz,Vejdelek

, p. 462 - 467 (2007/10/12)

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