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692-56-8

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692-56-8 Usage

Physical state

Colorless liquid

Primary use

Reagent in organic synthesis

Reaction with aldehydes and ketones

Forms hydrazones, important intermediates in the production of pharmaceuticals and other organic compounds

Protective agent

Shields sensitive functional groups during chemical reactions

Reactivity

Reactive nature

Health hazards

Potential health hazards

Handling

Should be handled with care and used in a controlled laboratory environment

Check Digit Verification of cas no

The CAS Registry Mumber 692-56-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 692-56:
(5*6)+(4*9)+(3*2)+(2*5)+(1*6)=88
88 % 10 = 8
So 692-56-8 is a valid CAS Registry Number.

692-56-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-bis(trimethylsilyl)hydrazine

1.2 Other means of identification

Product number -
Other names bis-1,2-trimethylsilylhydrazine

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:692-56-8 SDS

692-56-8Relevant articles and documents

SILYL-NITROGEN COMPOUNDS I. REACTIONS OF DILITHIUM BIS(TRIMETHYLSILYLL)HYDRAZINE WITH GROUP IV HALIDES

Vasisht, Sham Kumar,Sood, Mohini,Sood, Nirupma,Singh, Gursharan

, p. 15 - 26 (2007/10/02)

Dilithium 1,2-bis(trimethylsilyl)hydrazine (1) reacts with CCl4, Me3SiCCl3 and CBr4 to form predominantly bis(trimethylsilyl)aminocarbonimidic dichloride, bis(trimethylsilyl)aminoisocyanide and bis(trimethylsilyl)diazene, whereas similar reactions with HCCl3, HCI3, H2CCl2, H2CI2, C2H4Cl2 or C2H2Cl4 lead to increasing amounts of bis(trimethylsilyl)hydrazine.In addition to the hydrazone, (Me3Si)2N-N=CH(Cl), the reaction of 1 with CHCl3 forms a small amount of triazasilacyclopentane,.............. .In contrast, Me2SnCl2 reacts with 1 to give tetraazadistannacyclohexane (Me2Sn(NSiMe3)2)2, whereas SnCl4, SnCl2 and PbCl2 act mainly as oxidants and Me2SiCl2 forms polymers.Another product of the reaction of 1 with SnCl2 or PbCl2 is LiN(SiMe3)2 originating perhaps from LiNH(SiMe3) or (LiNN(SiMe3)2)2.

Darstellung silylierter Lithium-tetrazenide

Wiberg, Nils,Bayer, Heiner,Vasisht, Sham Kumar

, p. 2658 - 2660 (2007/10/02)

Reactions of butyllithium with tris- or bis(trimethylsilyl)tetrazene, (Me3Si)3N4H or (Me3Si)2N4H2, lead to tetrazenides 1 - 3 which are sensitive in hydrolysis and thermolysis as well as against oxygen.Reactions (1) - (6) refer to their modes of thermolysis.

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