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64778-72-9

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64778-72-9 Usage

General Description

2-[3,5-dimethoxy-4-(propan-2-yloxy)phenyl]ethanamine, also known as 25D-NBOMe, is a powerful psychedelic drug that belongs to the phenethylamine class. It is structurally similar to the psychedelic drug 2C-I, and is known for its potent hallucinogenic effects. 25D-NBOMe acts as a partial agonist at the 5-HT2A receptor, and is known to produce visual and auditory hallucinations, as well as altered perceptions of time and space. It is often sold on the street as a designer drug and is associated with serious side effects, including agitation, seizures, and even death in some cases. Due to its high potency and associated risks, 25D-NBOMe is classified as a Schedule I controlled substance in the United States.

Check Digit Verification of cas no

The CAS Registry Mumber 64778-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,7,7 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 64778-72:
(7*6)+(6*4)+(5*7)+(4*7)+(3*8)+(2*7)+(1*2)=169
169 % 10 = 9
So 64778-72-9 is a valid CAS Registry Number.

64778-72-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,5-dimethoxy-4-propan-2-yloxyphenyl)ethanamine

1.2 Other means of identification

Product number -
Other names Isoproscaline

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:64778-72-9 SDS

64778-72-9Downstream Products

64778-72-9Relevant articles and documents

Lipophilicity and serotonin agonist activity in a series of 4 substituted mescaline analogues

Nichols,Dyer

, p. 299 - 301 (2007/10/06)

Replacement of the 4 methoxy of mescaline with higher alkyl homologues or with bromine led to increased activity at serotonin receptors in a sheep umbilical artery preparation. This activity appears correlated with lipophilicity, as measured by 1 octanol water partition coefficients, but drops off when the 4 substituent is about five atoms in length. It is suggested that 3,4,5 trisubstitution may give compounds which are as active as those with the 2,4 5 substitution pattern.

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