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72822-01-6

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Chemical Properties

Off-White to Beige Solid

Check Digit Verification of cas no

The CAS Registry Mumber 72822-01-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,8,2 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 72822-01:
(7*7)+(6*2)+(5*8)+(4*2)+(3*2)+(2*0)+(1*1)=116
116 % 10 = 6
So 72822-01-6 is a valid CAS Registry Number.
InChI:InChI=1/C19H26N2OS/c1-3-7-21-11-13(12-23(2)22)8-16-15-5-4-6-17-19(15)14(10-20-17)9-18(16)21/h4-6,10,13,16,18,20H,3,7-9,11-12H2,1-2H3/t13-,16?,18-,23?/m1/s1

72822-01-6 Well-known Company Product Price

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  • (1510867)  Pergolide sulfoxide  United States Pharmacopeia (USP) Reference Standard

  • 72822-01-6

  • 1510867-50MG

  • 5,764.59CNY

  • Detail

72822-01-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (6aR,9R)-9-(methylsulfinylmethyl)-7-propyl-6,6a,8,9,10,10a-hexahydro-4H-indolo[4,3-fg]quinoline

1.2 Other means of identification

Product number -
Other names Pergolide sulfoxide

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:72822-01-6 SDS

72822-01-6Upstream product

72822-01-6Downstream Products

72822-01-6Relevant articles and documents

Microbial transformations of pergolide to pergolide sulfoxide and pergolide sulfone

Smith,Davis,Kerr

, p. 733 - 736 (1983)

Fifty-eight microorganisms were investigated for their ability to effect the biotransformation of the ergoline alkaloid pergolide. A majority of these organisms formed pergolide sulfoxide, and a Helminthosporium species was investigated in greater detail since it yielded significant amounts of pergolide sulfoxide. A preparative-scale transformation afforded material which was identified as the sulfoxide based on melting point, spectral, and chromatographic comparison with authentic material as well as its conversion to pergolide by reduction with triphenylphosphine. An analytical high-performance liquid chromatographic determination of the enzymatic versus spontaneous air-oxidation of pergolide in growing cultures and controls showed negligible air-oxidation and an ~40% enzymatic conversion of pergolide to the sulfoxide. Several organisms, including Aspergillus alliaceus, formed a second metabolite, pergolide sulfone, which was identified on the basis of co-chromatographic data.

6-N-Propyl-8-methoxymethyl or methylmercaptomethylergolines and related compounds

-

, (2008/06/13)

6-n-Propyl (ethyl or allyl)-8β-methoxy-(methylsulfinyl, methylsulfonyl, or methylmercapto) methylergolines, 8-ergolenes or 9-ergolenes, useful as prolactin inhibitors and in the treatment of Parkinsonism.

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