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80664-09-1

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80664-09-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80664-09-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,6,6 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 80664-09:
(7*8)+(6*0)+(5*6)+(4*6)+(3*4)+(2*0)+(1*9)=131
131 % 10 = 1
So 80664-09-1 is a valid CAS Registry Number.

80664-09-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-(3-iodophenyl)guanidine

1.2 Other means of identification

Product number -
Other names (m-iodophenyl)guanidine

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:80664-09-1 SDS

80664-09-1Downstream Products

80664-09-1Relevant articles and documents

Adrenal medulla imaging agents: A structure-distribution relationship study of radiolabeled aralkylguanidines

Wieland,Mangner,Inbasekaran,Brown,Wu

, p. 149 - 155 (2007/10/02)

Fourteen 125I-labeled aralkylguanidines were synthesized and evaluated as potential imaging agents for the adrenal medullae and tumors of adrenomedullary origin. These guanidines are radiotracer analogues of guanethidine, an antihypertensive agent thought to mediate neuron blockade by uptake into adrenergic nerves. Dog adrenal medullae were used as a model to test radiotracer affinity for catecholamine storage tissue. Tissue distribution studies revealed that a number of radioiodinated guanidines showed pronounced localization in the adrenal medullae following intravenous injection, in certain cases exceeding that of either (-)-[3H]norepinephrine or [14C]guanethidine. (m-[125I]Iodobenzyl)guanidine (m-IBG) gave the best combination of high concentration and selectivity. The low adrenomedullary affinity observed with [14C]guanidine and m-[125I]iodobenzylamine demonstrates the --- -------------- uniqueness of the aralkylguanidine structure. Preliminary evidence suggests that m-IBG is a storage analogue of norepinephrine. A second 125I-aralkylguanidine is now being used clincally in imaging and radiotherapy of catecholamine tumors, such as pheochromocytoma.

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