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24335-35-1

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24335-35-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24335-35-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,3 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24335-35:
(7*2)+(6*4)+(5*3)+(4*3)+(3*5)+(2*3)+(1*5)=91
91 % 10 = 1
So 24335-35-1 is a valid CAS Registry Number.

24335-35-1SDS

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 1,3-ditert-butyl-2,4-dichloro-1,3,2,4-diazadiphosphetidine

1.2 Other means of identification

Product number -
Other names 1,3,2,4-Diazadiphosphetidine,2,4-dichloro-1,3-bis(1,1-dimethylethyl)

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:24335-35-1 SDS

24335-35-1Upstream product

24335-35-1Relevant articles and documents

Reactions of Lithio-aminofluorosilanes with Covalent Element Halides

Neemann, Jutta,Klingebiel, Uwe

, p. 527 - 535 (2007/10/02)

Halides of boron, germanium, phosphorus, and arsenic react with lithio-aminofluorosilanes (1a-e) with elimination of lithium halide and substitution (to 2a, b, 3c, 4b, 5b, 5d, 6b).Depending on the bulkiness of the substituents and the reaction conditions, halosilanes are also cleaved off and four-membered rings (8d, 10b, 11b, 13b, 14b) are formed.The reaction of 1e with (Me3Si)2NPF2 leads to the formation of the aminoiminophosphane 9e.A 1,3-migration of a silyl group from the alkyl- to the arylamino-nitrogen is observed in this reaction. 5d reacts with lithiated (2,4,6-trimethylphenyl)(trimethylsilyl)amine to give 15d and LiF.The aminoiminophosphane 16d is obtained by thermal difluorosilane elimination from 15d.An aminoiminodifluorophosphane (12b) is formed in the reaction of 1b with PF5, isobutene, tert-butyldifluorophenylsilane, and LiF being claved off.

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