Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

S178

Sigma-Aldrich

(R)-SKF-82957 hydrobromide

solid

Synonym(s):

(1R)-6-Chloro-2,3,4,5-tetrahydro-3-methyl-1-phenyl-1H-3-benzazepine-7,8-diol hydrobromide, 1H-3-Benzazepine-7,8-diol,6-chloro-2,3,4,5-tetrahydro-3-methyl-1-phenyl hydrobromide hydrobromide

Sign Into View Organizational & Contract Pricing

Select a Size

5 MG
$660.00

$660.00


In StockDetails


Request a Bulk Order

Select a Size

Change View
5 MG
$660.00

About This Item

Empirical Formula (Hill Notation):
C17H18ClNO2 · HBr
CAS Number:
Molecular Weight:
384.70
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77

$660.00


In StockDetails


Request a Bulk Order

form

solid

Quality Level

optical activity

[α]22/D +22.46°, c = 0.76 in DMF(lit.)

color

white

solubility

H2O: 7.5 mg/mL
DMSO: soluble

SMILES string

Br[H].CN1CCc2c(Cl)c(O)c(O)cc2[C@H](C1)c3ccccc3

InChI

1S/C17H18ClNO2.BrH/c1-19-8-7-12-13(9-15(20)17(21)16(12)18)14(10-19)11-5-3-2-4-6-11;/h2-6,9,14,20-21H,7-8,10H2,1H3;1H/t14-;/m1./s1

InChI key

BCZHWHQKKPEORG-PFEQFJNWSA-N

Biochem/physiol Actions

Selective D1 dopamine receptor agonist.

Caution

hygroscopic, photosensitive

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

F R Pfeiffer et al.
Journal of medicinal chemistry, 25(4), 352-358 (1982-04-01)
6-Chloro-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepines were synthesized and evaluated as agonists of central and peripheral dopamine receptors. These benzazepines were prepared by cyclization of certain amino alcohols followed by demethylation of the 7,8-dimethoxy groups of the precursors to the 7,8-catecholic moiety. Preliminary evidence of
P H Andersen et al.
European journal of pharmacology, 188(6), 335-347 (1990-06-12)
Dopamine receptor selectivity was investigated for a number of dopamine receptor agonists. In vitro, the benzazepine derivatives, e.g., SKF 38393 and SKF 75670 as well as the isoquinoline derivatives, SKF 89626 and SKF 89615, were D1 receptor-selective. All other compounds

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service