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4833-42-5

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4833-42-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4833-42-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,3 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4833-42:
(6*4)+(5*8)+(4*3)+(3*3)+(2*4)+(1*2)=95
95 % 10 = 5
So 4833-42-5 is a valid CAS Registry Number.

4833-42-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dicyclohexyl-3-phenylguanidine

1.2 Other means of identification

Product number -
Other names N-phenyl-N',N''-diicyclohexylguanidine

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:4833-42-5 SDS

4833-42-5Downstream Products

4833-42-5Relevant articles and documents

Two unprecedented aromatic guanidines supramolecular chains self-assembled by hydrogen bonding interaction

Zhang, Yunshen,Huang, Yichao,Zhang, Jiangwei,Zhu, Li,Chen, Kun,Hao, Jian

, p. 145 - 150 (2015)

Two aromatic guanidine derivatives, C6H5N = C(NHCy)2 (1), (n-TBA)C6H5NHC(NHCy)2Mo2O7 (2) (Cy = cyclohexyl), were synthetized with high yields. Both of them self-assemb

Nanoparticulate copper(II) oxide catalyzed synthesis of guanidine derivatives and their conversion into functionalized iminoguanidines

Yavari, Issa,Sodagar, Esmat,Nematpour, Manijeh,Askarian-Amiri, Mohammad

, p. 1230 - 1232 (2015)

Abstract A simple synthesis of functionalized iminoguanidines from N-sulfoketenimines and N,N′,N′′-trisubstituted guanidines, generated by nanoparticulate copper(II) oxide-catalyzed hydroamination of di(cyclo)alkylcarbodiimides, is described.

Combination of air/moisture/ambient temperature compatible organolithium chemistry with sustainable solvents: Selective and efficient synthesis of guanidines and amidines

Anti?olo, Antonio,Carrillo-Hermosilla, Fernando,Elorriaga, David,García-álvarez, Joaquín,Parra-Cadenas, Blanca

supporting information, p. 800 - 812 (2022/02/02)

Highly-efficient and selective fast addition of in situ generated lithium amides [LiN(H)R] (obtained via an acid-base reaction between n-BuLi and the desired primary amine) into carbodiimides (R-NCN-R) or nitriles (R-CN) has been studied, for the first ti

Synthesis and Reactivity of NNNNN-Pincer Multidentate Pyrrolyl Rare-Earth-Metal Amido-Chloride or Dialkyl Complexes

Cui, Peng,Du, Jun,Huang, Zeming,Sheng, Weiming,Wang, Shaowu,Wei, Yun,Xu, Xiaolong,Zhang, Lijun,Zhang, Xiuli,Zhou, Shuangliu,Zhu, Xiancui

supporting information, p. 4525 - 4534 (2020/12/22)

The NNNNN-pincer multidentate pyrrolyl rare-earth-metal amido-chloride complexes {η1:κ3-2,5-[CH3N(CH2CH2)2NCH2]2C4H2N}RECl[N(SiMe3)2] (RE = Y (2a), Sm (2b), Dy (2c), Er (2d), Yb (2e)) were synthesized by one step from reactions of [(Me3Si)2N]3RE(μ-Cl)Li(T

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