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151515-23-0

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151515-23-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 151515-23-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,5,1 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 151515-23:
(8*1)+(7*5)+(6*1)+(5*5)+(4*1)+(3*5)+(2*2)+(1*3)=100
100 % 10 = 0
So 151515-23-0 is a valid CAS Registry Number.

151515-23-0SDS

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 1,3-diisopropyl-4,5-dimethyl-2,3-dihydro-1H-imidazol-2-ylidene

1.2 Other means of identification

Product number -
Other names 1,3-diisopropyl-4,5-dimethyl-2,3-dihydroimidazol-2-ylidene

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:151515-23-0 SDS

151515-23-0Upstream product

151515-23-0Relevant articles and documents

Indirect Access to Carbene Adducts of Bismuth- And Antimony-Substituted Phosphaketene and Their Unusual Thermal Transformation to Dipnictines and [(NHC)2OCP][OCP]

Walley, Jacob E.,Warring, Levi S.,Kertész, Erik,Wang, Guocang,Dickie, Diane A.,Benk?, Zoltán,Gilliard, Robert J.

, p. 4733 - 4743 (2021)

The synthesis and thermal redox chemistry of the first antimony (Sb)- and bismuth (Bi)-phosphaketene adducts are described. When diphenylpnictogen chloride [Ph2PnCl (Pn = Sb or Bi)] is reacted with sodium 2-phosphaethynolate [Na[OCP]·(dioxane)x], tetraphe

Stabilization of a transient diorganogermylene by an N-heterocyclic carbene

Rupar, Paul A.,Jennings, Michael C.,Ragogna, Paul J.,Baines, Kim M.

, p. 4109 - 4111 (2008/10/09)

The synthesis of a carbene-stabilized transient germylene is presented; the resulting complex liberates free germylene upon heating, forms a stable adduct with BH3, and reacts with MeLi to displace the carbene.

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