Welcome to LookChem.com Sign In|Join Free
  • or
2-(benzylcarbamimidoyl)-1-hydroxy-1-oxodiazanium is a complex organic compound with the chemical formula C8H10N3O3. It is a derivative of diazanium, featuring a benzylcarbamimidoyl group attached to the 2-position. 2-(benzylcarbamimidoyl)-1-hydroxy-1-oxodiazanium is characterized by its hydroxyl and oxo groups, which contribute to its reactivity and potential applications in chemical synthesis. It is an intermediate in the formation of certain pharmaceuticals and may be involved in the synthesis of compounds with biological activity. The compound's structure and properties make it a subject of interest in organic chemistry, particularly in the development of new drugs and other chemical products.

5415-72-5

Post Buying Request

5415-72-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

5415-72-5 Usage

Type of compound

Positively charged organic molecule.

Key functional groups

Diazanium group, hydroxy group, benzylcarbamimidoyl group.

Synthesis purpose

Pharmaceutical research and drug development.

Potential properties

Biological activities and interactions with biological systems.

Possible applications

Medicinal chemistry, development of new drugs.

Research status

Further research needed to understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 5415-72-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5415-72:
(6*5)+(5*4)+(4*1)+(3*5)+(2*7)+(1*2)=85
85 % 10 = 5
So 5415-72-5 is a valid CAS Registry Number.

5415-72-5SDS

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 2-benzyl-1-nitroguanidine

1.2 Other means of identification

Product number -
Other names N-Benzyl-N-nitro-guanidin

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:5415-72-5 SDS

5415-72-5Relevant academic research and scientific papers

Design, Synthesis, and Antifungal Activity of Sulfoximine Derivatives Containing Nitroguanidine Moieties

Li, Hongsen,Li, Ya,Liu, Yuan,Shao, Qun,Xiao, Yulong,Xie, Yonghai,Zhao, Linjing

, (2022/02/16)

To discover novel pesticide candidates, a series of sulfoximine derivatives were designed and synthesized via the oxidation coupling reaction of sulfides and N-alkyl nitroguanidines. The compounds were evaluated for their antifungal activity against six phytopathogenic fungi. Most of them exhibited a broad spectrum of fungicidal activity in vitro. Compound 8IV-b displayed good fungicidal activity against Sclerotinia sclerotiorum, Rhizoctonia solani, Botrytis cinerea, Fusarium graminearum, and Phytophthora capsici, with EC50 value of 12.82, 12.50, 17.25, 31.08, and 30.11 mg/L, respectively. In addition, compounds 8III-c and 8IV-e had EC50 values of 22.23 and 20.67 mg/L against P. capsic, which were significantly better than that of the commercial procymidone (118.15 mg/L). Strikingly, 8IV-d exhibited satisfactory fungicidal activity against B. cinerea, which was comparable to control procymidone in terms of their EC50 values (7.42 versus 10.83 mg/L), and the bioassays in vivo further confirmed that 8IV-d possessed potent protective effect against B. cinerea at 200 mg/L (72.2 %). These present findings will facilitate the design and development of novel potent fungicides.

Nitroguanidine compound and preparation and application thereof

-

Paragraph 0033-0035; 0054-0055, (2020/04/02)

The invention relates to a nitroguanidine compound and preparation and application thereof. The nitroguanidine compound is a compound with a structure as shown in a general formula (I) which is described in the specification, or a pharmaceutically acceptable salt, enantiomer, diastereoisomer, tautomer, solvate, polymorphic substance or prodrug thereof. In the general formula (I), R1 is one selected from the group consisting of C1-C8 saturated or unsaturated aliphatic group, a benzyl group, a substituted benzyl group and a substituted pyridylmethyl group; and R2 is one selected from the group consisting of a C1-C8 saturated or unsaturated aliphatic group, a phenyl group, a substituted phenyl group and a substituted pyridyl group. Compared with the prior art, the nitroguanidine compound disclosed by the invention has a relatively good prevention effect on agricultural fungal diseases such as fusarium, gibberella, stemphylium solani, phytophthora, pythium aphanidermatum, botrytis cinerea,sclerotinia sclerotiorum and rhizoctonia solani, and can be used as a potential plant bactericide.

Substituted nitro and cyanoguanidines and their use of increasing crop yields

-

, (2008/06/13)

Novel substituted phenyl and benzyl nitroguanidine and phenyl and benzyl cyanoguanidine compounds. Methods for increasing crop yield, inhibiting lodging of graminaceous crops, and inducing cytokinin-like responses in crop plants with said novel guanidine

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 5415-72-5