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10-Hped, also known as 10-Hydroxyphenethyldimethylamine or 10-Hydroxyphenethyl-N,N-dimethylamine, is a chemical compound with the molecular formula C10H15NO. It is a derivative of phenethylamine, a naturally occurring monoamine compound found in trace amounts in the human brain and various plants. 10-Hped is a synthetic substance that has gained attention for its potential psychoactive effects, although its pharmacological properties and safety profile are not well understood. It is important to note that the use and distribution of 10-Hped may be subject to legal restrictions due to its unregulated status and potential health risks.

2135-57-1

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2135-57-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2135-57-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,3 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2135-57:
(6*2)+(5*1)+(4*3)+(3*5)+(2*5)+(1*7)=61
61 % 10 = 1
So 2135-57-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H24O4/c1-17-8-7-15-13(14(17)4-5-16(17)20)3-2-11-10-12(19)6-9-18(11,15)22-21/h10,13-15,21H,2-9H2,1H3/t13-,14-,15-,17-,18?/m0/s1

2135-57-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (8S,9S,10S,13S,14S)-10-hydroperoxy-13-methyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-3,17-dione

1.2 Other means of identification

Product number -
Other names Estr-4-ene-3,17-dione,10-hydroperoxy

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:2135-57-1 SDS

2135-57-1Downstream Products

2135-57-1Relevant academic research and scientific papers

Biosynthesis of Estrogens bz Microsomal Placental Aromatase; Isolation and Metabolism of 10β-Hydroxyestr-4-ene-3,17-dione

Caspi, Eliahu,Dharmaratne, H. Ranjith W.,Shackleton, Cedric

, p. 1699 - 1700 (1989)

Incubation of -19-oxoandrost-4-ene-3,17-dione (2a) with microsomal aromatase gave inter alia -10β-hydroxyestr-4-ene-3,17-dione (1), whose analogue (1b) on incubation with the aromatase gave 10β,17β-dihydroxyestr-4-en-3-one (1d) (ca. 10percent) and no estrogens which would indicate that (1b) is not an obligatory estrogen precursor.

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