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705-98-6 Usage

Guanidine derivative

A compound derived from guanidine, which is a basic compound containing a central carbon atom bonded to four nitrogen atoms.

Benzyl group attachment

The benzyl group (C6H5CH2-) is attached to the oxygen atom in the compound.

Organic synthesis

1-(Benzyloxy)guanidine has been studied for its potential use as a reagent for the introduction of guanidine groups into organic molecules.

Pharmacological properties

The compound has been investigated for its potential as an antidiabetic agent and its potential as a treatment for cognitive disorders.

Antidiabetic agent

It has shown potential in managing or treating diabetes by improving insulin sensitivity or glucose metabolism.

Treatment for cognitive disorders

It has been explored for its potential to improve cognitive function or treat conditions such as Alzheimer's disease or other neurodegenerative disorders.

Metal catalyst ligand

1-(Benzyloxy)guanidine has shown potential as a ligand for metal catalysts, which are used to accelerate chemical reactions.

Precursor for organic compounds

The compound can be used as a starting material for the synthesis of other organic compounds.

Diverse applications

1-(Benzyloxy)guanidine has garnered interest for its potential applications in both the field of organic chemistry and pharmacology.

Check Digit Verification of cas no

The CAS Registry Mumber 705-98-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 705-98:
76 % 10 = 6
So 705-98-6 is a valid CAS Registry Number.



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


1.1 GHS Product identifier

Product name 2-phenylmethoxyguanidine

1.2 Other means of identification

Product number -
Other names 3-benzyloxy 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:705-98-6 SDS

705-98-6Relevant articles and documents



, (2010/12/30)

The present invention has its object to provide a curable composition which comprises a guanidine compound as a non-organotin type catalyst, is less discolored, has good surface curability, depth curability, strength rise and adhesiveness, and can retain the curability even after storage; the above object can be achieved by a curable composition which comprises: (A) an organic polymer containing a silyl group capable of crosslinking under siloxane bond formation, the silyl group being a group represented by the general formula (1): -SiX 3 (1) (wherein X represents a hydroxyl group or a hydrolyzable group and the three X groups may be mutually the same or different), (B) a guanidine compound (B-1) as a silanol condensation catalyst, and (C) a plasticizer, wherein the content of the component (B-1) is not lower than 0.1 part by weight but lower than 8 parts by weight per 100 parts by weight of the component (A), and a non-phthalate ester plasticizer accounts for 80 to 100% by weight of the (C) component plasticizer.

Reductive Cleavage of Hydroxylamine Derivatives by Dihydrolipoic Acid-Iron(II)

Nambu, Yoko,Kijima, Masashi,Endo, Takeshi,Okawara, Makoto

, p. 3066 - 3069 (2007/10/02)

The reduction of hydroxylamine derivatives was attempted with dihydrolipoic acid-iron(II) to obtain corresponding alcohols and amines in high yields under a mild condition (pH 9.1, 30 deg C).Some dithiols other than dihydrolipoic acid which cyclize to form disulfides were also useful for the reduction, and ferrous ion worked as an effective catalyst.From the spectroscopic and kinetic studies, the reduction was found to proceed through 1:1:1 complex formation among dihydrolipoic acid, ferrous ion, and N-O compounds.

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