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Spectinamine is a naturally occurring alkaloid compound found in the plant family Solanaceae, particularly in the genus Solanum. It is structurally similar to nicotine and belongs to the group of tropane alkaloids. Spectinamine has been studied for its potential biological activities, including its effects on the central nervous system, where it acts as a potent acetylcholine receptor agonist. This property makes it a subject of interest in research related to neurological disorders and as a potential therapeutic agent. However, it is important to note that spectinamine is also associated with certain toxic effects, and its presence in some plants can be harmful if ingested. The study of spectinamine and related compounds continues to provide insights into the complex chemistry and pharmacology of natural products.

6216-38-2

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6216-38-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6216-38-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,1 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6216-38:
(6*6)+(5*2)+(4*1)+(3*6)+(2*3)+(1*8)=82
82 % 10 = 2
So 6216-38-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H18N2O4/c1-9-3-5(11)4(10-2)7(13)8(14)6(3)12/h3-14H,1-2H3

6216-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-bis(methylamino)cyclohexane-1,2,3,5-tetrol

1.2 Other means of identification

Product number -
Other names N1,N3-bis-methylamino-1,3-dideoxy-myo-inositol

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:6216-38-2 SDS

6216-38-2Downstream Products

6216-38-2Relevant academic research and scientific papers

Polyfunctionalised Cyclohexanes from Dianhydroinositols. cis-1,3(1,4)-Inosadiamines from Benzene

Schubert, Juergen,Keller, Reinhold,Schwesinger, Reinhard,Prinzbach, Horst

, p. 2524 - 2545 (2007/10/02)

The preparative value of the dianhydroinositols 4 - 6, which are readily available from benzene, for the total synthesis of cis-1,4- and cis-1,3-disubstituted cyclohexanetetrols is demonstrated.With monovalent reagents (H2O, HI, NaN3, NH2NH2) the twofold epoxide opening proceeds regioselectively (1,4-disubstitution) yielding the muco- and chiro-cyclohexane derivatives 9, 17, and 26.With hydrazine and N,N'-dimethylhydrazine as 1,2-dinucleophiles the cis-1,3-inosadiamines 7 g (5-epistreptamine) and 16 g, j (2-epistreptamine, actinamine) are obtained from 4/5 in good yields (75 - 90percent).From the less symmetrical 6, however, only the mixture of 25 g (streptamine) and 27 g is produced in modest yield (ca. 50percent).The epoxide opening reactions starting from 4 - 6 are kinetically so similar that a selective opening is not possible.

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