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993-50-0 Usage

Chemical Properties

liquid; uses: a dehydrochlorinating agent [ALD94]

Check Digit Verification of cas no

The CAS Registry Mumber 993-50-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,9 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 993-50:
(5*9)+(4*9)+(3*3)+(2*5)+(1*0)=100
100 % 10 = 0
So 993-50-0 is a valid CAS Registry Number.
InChI:InChI=1/C2H6N.3CH3.Sn/c1-3-2;;;;/h1-2H3;3*1H3;/q-1;;;;+1/rC3H9Sn.C2H6N/c1-4(2)3;1-3-2/h1-3H3;1-2H3/q+1;-1

993-50-0 Well-known Company Product Price

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  • Aldrich

  • (429287)  (Dimethylamino)trimethyltin(IV)  technical grade

  • 993-50-0

  • 429287-5G

  • 1,931.67CNY

  • Detail

993-50-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-N-trimethylstannylmethanamine

1.2 Other means of identification

Product number -
Other names N,N-dimethylaminotrimethyltin

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:993-50-0 SDS

993-50-0Relevant articles and documents

ORGANOMETALLIC COMPOUNDS AND METHODS FOR THE DEPOSITION OF HIGH PURITY TIN OXIDE

-

Paragraph 0098, (2019/02/17)

Disclosed herein are compounds useful for the deposition of high purity tin oxide. Also disclose are methods for the deposition of tin oxide films using such compounds. Such films demonstrate high conformality, high etch selectivity and are optically transparent. Such compounds are those of the Formula as follows R x -Sn-A 4-x wherein: A is selected from the group consisting of (Y a R' z ) and a 3- to 7-membered N- containing heterocyclic group; each R group is independently selected from the group consisting of an alkyl or aryl group having from 1 to 10 carbon atoms; each R' group is independently selected from the group consisting of an alkyl, acyl or aryl group having from 1 to 10 carbon atoms; x is an integer from 0 to 4; a is an integer from 0 to 1; Y is selected from the group consisting of N, O, S, and P; and z is 1 when Y is O, S or when Y is absent and z is 2 when Y is N or P.

Organotin intercalation compounds of FeOCl: Synthesis, 57Fe and 119mSn M?ssbauer and infrared spectroscopy, and powder X-ray diffraction studies

Phillips,Herber

, p. 3081 - 3088 (2008/10/08)

Four new organotin intercalates of FeOCl were synthesized and studied by infrared and variable-temperature 57Fe and 119mSn M?ssbauer spectroscopies and by X-ray powder diffraction. These systems were chosen to provide a detailed microscopic spectroscopic examination of both the host and the guest species as well as a comprehensive picture of the guest-host interaction. The neat organotins, 4-(CH3)3Sn(C5H4N) (P1), (CH3)3SnN(CH3)2 (A1), (CH3)2Sn[N(CH3)2]2 (A2), and Sn[N(CH3)2]4 (A4), all show evidence for an increase in tin coordination upon intercalation to form nominally FeOCl(P1)1/7.5 (INP1), FeOCl(A1)1/5.5 (INA1), FeOCl(A2)1/8 (INA2), and FeOCl(A4)1/16 (INA4). The intercalation process is described as a redox process where an electron is first donated to the FeOCl lattice with the corresponding formation of a pyridinium ligand for INP1 and an iminium ligand for INA1, INA2, and INA4, which then enter between the layers of the FeOCl matrix. The intercalated species in INP1 is described as an associated moiety with both four- and five-coordinate tin and an abnormally low charge transfer to the lattice, which is attributed to the large size of the guest. Data for INA1, INA2, and INA4 are interpreted in terms of six-coordinate tin species in which the fifth and sixth sites are lattice chlorines. An additional organic intercalation compound, FeOCl-[(CH3)2N+=CH2] 1/5[Cl-]1/10, was also prepared and studied as a model compound for the intercalation of the organotin amines. 57Fe M?ssbauer relaxation calculations have been used to determine the extent of the charge transfer to the lattice.

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