Welcome to LookChem.com Sign In|Join Free
  • or
Triethylstannanylium (oxomethylidene)azanide is a complex organic compound with the chemical formula [Et3Sn=C=N]-. It is a derivative of the azide ion (N3-), where one of the nitrogen atoms is replaced by a carbon atom, forming an imidoyl group (C=N). The triethylstannanylium (Et3Sn+) moiety is a positively charged group consisting of a tin atom bonded to three ethyl groups. triethylstannanylium (oxomethylidene)azanide is of interest in organometallic chemistry due to its unique structure and potential applications in the synthesis of various organometallic compounds. It is also known for its reactivity and can participate in various chemical reactions, such as insertion reactions, where it can add across double bonds. The compound's stability and reactivity make it a subject of study in the development of new synthetic methods and materials.

757-36-8

Post Buying Request

757-36-8 Suppliers

Recommended suppliers

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

757-36-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 757-36-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,5 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 757-36:
(5*7)+(4*5)+(3*7)+(2*3)+(1*6)=88
88 % 10 = 8
So 757-36-8 is a valid CAS Registry Number.

757-36-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name triethyl(isocyanato)stannane

1.2 Other means of identification

Product number -
Other names triethyisocyanatostannane

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:757-36-8 SDS

757-36-8Downstream Products

757-36-8Relevant academic research and scientific papers

1-(Trialkylstannylthioalkyl)silatranes

Sorokin,Stankevich,Kuznetsova,Lopyrev,Voronkov

, p. 560 - 563 (2007/10/03)

Two methods of synthesis of 1-(trialkylstannylthioalkyl)silatranes R3SnS(CH2)nSi(OCH2CH2)3N (n = 1, 2) have been developed. The first method involves transetherification of corresponding trimethoxysilanes with tris(2-hydroxyethyl)amine, and the second is based on reaction of sulfur-containing 1-organylsilatranes of the general formula RS(CH2)nSi(OCH2CH2)3N, where R = H, N≡C, MeCO, EtOC(S), with trialkylalkoxystannanes or hexaethyldistannoxane. Reaction of 1-(triethylstannylthiomethyl)silatrane Et3SnS· CH2Si(OCH2CH2)3N with excess MeI involves cleavage of the Sn-S bond and results in formation of triethyl-iodostannane and dimethyl(1-silatranylmethyl)sulfonium iodide. Antimicrobial activity of the products has been studied.

Trialkyl(alkenylthio)stannanes

Voronkov, M. G.,Dubinskaya, E. I.,Legov, G. N.,Stankevich, O. S.,Protasova, L. E.,et al.

, p. 2031 - 2034 (2007/10/02)

Previously unknown trialkyl(alkenylthio)stannanes were obtained by the interaction of alkenyl thiocyanates with trialkyl(methoxy)stannanes; some of their properties and transformations were studied. - Key words: trialkyl(alkenylthio)stannanes; alkenyl thi

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 757-36-8