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75614-93-6

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75614-93-6 Usage

Uses

(S)-(+)-alpha-Methylhistamine Dihydrobromide is an H3 receptor agonist.

Biological Activity

Less active enantiomer of H 3 agonist R-(-)- α -methylhistamine ((R)-(-)-a-Methyl-1H-imidazole-4-ethanaminedihydrobromide ); 120-fold less potent than R-(-) at H 3 .

Check Digit Verification of cas no

The CAS Registry Mumber 75614-93-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,6,1 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 75614-93:
(7*7)+(6*5)+(5*6)+(4*1)+(3*4)+(2*9)+(1*3)=146
146 % 10 = 6
So 75614-93-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H11N3.2BrH/c1-5(7)2-6-3-8-4-9-6;;/h3-5H,2,7H2,1H3,(H,8,9);2*1H/t5-;;/m0../s1

75614-93-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-1-(1H-imidazol-5-yl)propan-2-amine,dihydrobromide

1.2 Other means of identification

Product number -
Other names 8-CPT-2Me-cAMP,sodium salt

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:75614-93-6 SDS

75614-93-6Downstream Products

75614-93-6Relevant articles and documents

Histamine analogues. 32nd communication: synthesis and pharmacology of sopromidine, a potent and stereoselective isomer of the achiral H2-agonist impromidine

Elz, Sigurd,Gerhard, Guenter,Schunack, Walter

, p. 259 - 262 (2007/10/02)

Synthesis and pharmacology of sopromidine ((R)-7) and (S)-7, 2 position isomers of impromidine derived from the enantiomeric α-methylhistamines, are reported.The enantiomers of 7 show high stereoselectivity at the atrial H2-receptor of the guinea-pig. (R)-7 is revealed to be a full H2-agonist with 7.4-fold potency relative to histamine, while (S)-7 is a competitive H2-antagonist. chiral H2-agonists / histamine H2-receptor / impromidine analogues / α-methylhistamine

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