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280-05-7

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280-05-7 Usage

Description

Pseudohyoscyamine, also known as scopolamine, is a naturally occurring alkaloid derived from the plant genus Hyoscyamus. It is a secondary metabolite with a complex chemical structure, characterized by its tropane core. Pseudohyoscyamine exhibits various pharmacological properties, making it a versatile compound with potential applications in different fields.

Uses

Used in Pharmaceutical Industry:
Pseudohyoscyamine is used as a pharmaceutical compound for its antispasmodic, sedative, and anticholinergic properties. It is particularly effective in treating gastrointestinal disorders, such as irritable bowel syndrome and peptic ulcers, by reducing smooth muscle spasms and secretion of gastric acid.
Used in Cosmetic Industry:
In the cosmetic industry, pseudohyoscyamine is used as an active ingredient in anti-aging and skin care products. Its anti-inflammatory and anticholinergic properties help to reduce wrinkles, improve skin elasticity, and provide a tightening effect on the skin.
Used in Chemical Synthesis:
Pseudohyoscyamine is used as a reactant in the preparation of enantiomerically pure pseudohyoscyamine derivatives. These derivatives have potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science, due to their unique stereochemistry and biological activities.
Used in Drug Delivery Systems:
Similar to gallotannin, pseudohyoscyamine can also be incorporated into drug delivery systems to enhance its bioavailability, targeting, and therapeutic efficacy. Nanoparticle-based drug delivery systems, such as liposomes, polymeric nanoparticles, and metallic nanoparticles, can be employed to improve the delivery of pseudohyoscyamine to specific tissues or cells, thereby increasing its therapeutic potential and reducing side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 280-05-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,8 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 280-05:
(5*2)+(4*8)+(3*0)+(2*0)+(1*5)=47
47 % 10 = 7
So 280-05-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H13N/c1-2-6-4-5-7(3-1)8-6/h6-8H,1-5H2

280-05-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-Azabicyclo(3.2.1)octane

1.2 Other means of identification

Product number -
Other names -

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:280-05-7 SDS

280-05-7Relevant articles and documents

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Laube et al.

, p. 670,673 (1977)

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Efficient oxidation of alcohols electrochemically mediated by azabicyclo-N-oxyls

Demizu, Yosuke,Shiigi, Hirofumi,Oda, Takahisa,Matsumura, Yoshihiro,Onomura, Osamu

, p. 48 - 52 (2008/09/17)

Preparation of azabicyclo-N-oxyls and the electrochemical oxidation of alcohols using them as mediators have been exploited. This oxidation was applicable to a transformation of sterically hindered secondary alcohols into the corresponding ketones in high yields.

Fused azabicyclic compounds that inhibit vanilloid receptor subtype 1 (VR1) receptor

-

, (2008/06/13)

Compounds of formula (I) are novel VR1 antagonists that are useful in treating pain, inflammatory thermal hyperalgesia, urinary incontinence and bladder overactivity, wherein X1, X2, X3, X4, X5, R5, R6, R7, R8a, R8b, R9, Z1, Z2 and L are as defined in the description.

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