15075-90-8

• 

• Basic information

  1. Product Name: 1,2-DICHLOROETHYLENE-D2
  2. Synonyms: 1,2-DICHLOROETHYLENE (1,2-D2);1,2-DICHLOROETHYLENE-D2
  3. CAS NO:15075-90-8
  4. Molecular Formula: C₂H₂Cl₂
  5. Molecular Weight: 98.96
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 15075-90-8.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: 1,2-DICHLOROETHYLENE-D2(CAS DataBase Reference)
  10. NIST Chemistry Reference: 1,2-DICHLOROETHYLENE-D2(15075-90-8)
  11. EPA Substance Registry System: 1,2-DICHLOROETHYLENE-D2(15075-90-8)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 15075-90-8(Hazardous Substances Data)

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• SDS
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• Article

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• MEPERIDINE (D4)

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• Henan Allgreen Chemical Co.,Ltd
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• Ethylene-1,2-d2,1,2-dichloro- (8CI)

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• Henan Tianfu Chemical Co., Ltd.
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• 1,2-DICHLOROETHYLENE-D2CAS

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• Hangzhou Fandachem Co.,Ltd
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• Ethylene-1,2-d2,1,2-dichloro- (8CI)

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• yuyongmei
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• Ethylene-1,2-d2,1,2-dichloro- (8CI)

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• Clearsynth Labs Limited
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15075-90-8 Usage

General Description

1,2-Dichloroethene-D2 is a chemical compound that is also known as deuterated 1,2-Dichloroethylene. It is a heavy isotopic form of 1,2-Dichloroethylene, which is a colorless liquid with a sweet odor. 1,2-Dichloroethene-D2 is used as a solvent and in the manufacture of other chemicals, as well as in the production of plastics. It is also used in the production of adhesives, and as a solvent for aerosol formulations. The compound is also used in the production of rubber and adhesives. It is classified as a hazardous substance, and exposure to high levels of 1,2-Dichloroethene-D2 can cause irritation to the skin, eyes, and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 15075-90-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,7 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15075-90:
(7*1)+(6*5)+(5*0)+(4*7)+(3*5)+(2*9)+(1*0)=98
98 % 10 = 8
So 15075-90-8 is a valid CAS Registry Number.

15075-90-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	1,2-DICHLOROETHYLENE-D2

1.2 Other means of identification

Product number	-
Other names	-

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:15075-90-8 SDS

15075-90-8Upstream product

• 98815-02-2 6,6,6-tris(dimethylphenylphosphine)-6-hydrido-6-Re-nido-B₉H₁₂-9-OEt 

15075-90-8Downstream Products

15075-90-8Relevant articles and documents

Preparation, Structure, and Nuclear Magnetic Resonance Properties of the Nine-vertex nido-Rhenaborane and Some Related Chemistry

Beckett, Michael A.,Bown, Mark,Fontaine, Xavier L. R.,Greenwood, Norman N.,Kennedy, John D.,Thornton-Pett, Mark

, p. 1969 - 1982 (2007/10/02)

Thermolysis of (1) in C2D2Cl4 solution gives the new, pale yellow air-stable compound (2) in 80 percent yield.Crystals of the CH2Cl2 hemisolvate of (2) are monoclinic, space group P21/c, with a = 1130.0(3), b = 1292.2(3), c = 2424.0(5) pm, β = 94.15(2) degree, and Z = 4; the molecular structure was refined to R = 0.0399, R' = 0.0454.The detailed n.m.r. behaviour of compound (2) together with data for previously reported rhodium and iridium analogues permits the location of the substituent site on previously unconfirmed and thence provides information on mechanistic pathways for the formation of these and related metallaboranes.Detailed n.m.r. data for the non-metalla analogues - and previously unassigned - provide information on their mechanism of formation and a comparison with the metallaborane analogues.The n.m.r. work includes extensive use of - COSY and - COSY experiments and establishes general points.

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