Welcome to LookChem.com Sign In|Join Free

CAS

  • or

51775-36-1

Post Buying Request

51775-36-1 Suppliers

Recommended suppliersmore

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

51775-36-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51775-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,7,7 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51775-36:
(7*5)+(6*1)+(5*7)+(4*7)+(3*5)+(2*3)+(1*6)=131
131 % 10 = 1
So 51775-36-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H11Cl7/c11-2-8(3-12)5-1-10(16,17)9(8,4-13)7(15)6(5)14/h5-7H,1-4H2

51775-36-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,5,5-tetrachloro-4,7,7-tris(chloromethyl)bicyclo[2.2.1]heptane

1.2 Other means of identification

Product number -
Other names 5-endo,6-exo-2,2,5,6-Tetrachloro-1,7,7-tris(chloromethyl)-bicyclo(2.2.1)heptane

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:51775-36-1 SDS

51775-36-1Downstream Products

51775-36-1Relevant articles and documents

Khalifa et al.

, p. 653,655, 657 (1974)

Synthesis of two major toxaphene components and their photostabilities

Coelhan, Mehmet,Maurer, Martin

, p. 10105 - 10112 (2007/10/03)

The synthesis of 2-endo,3-exo,5-endo,6-exo,8,9,10-heptachlorobornane (B7-1001, Hp-Sed) and 2-endo,3-exo,5-endo,6-exo,8,9,9,10-octachlorobornane (B8-1412) is described. Both compounds are components of toxaphene, an insecticide that has been widely used in the past. B7-1001 is an important toxaphene congener, comprising up to 99% of total toxaphene concentrations found in fish and sediment samples from treated lakes. B8-1412 is also a significant component of toxaphene contamination in samples from biota. In synthesizing the compounds, 2-exo,3-endo,6-endo,8,9,10-hexachlorobornane (B6-913) was obtained by reduction of the well-known toxaphene component P 32 (B7-515, 2,2,5-endo,6-exo,8,9,10-heptachlorobornane), which was itself isolated from the chlorination products of (+)-camphene. Chlorination of B6-913 provided B7-1001 in 49.5% yield, and P 32 and four other heptachlorobornanes were also detected in the reaction mixture. Structures of two of the heptachlorobornanes were elucidated by MS and NMR as 2-exo,3-endo,6-endo,8,9,9,10-heptachlorobornane (B7-1461) and 2-exo,3,3,6-encto,8,9,10-heptachlorobornane (B7-1303). B8-1412 was isolated from the product mixture obtained by chlorination of 2-exo,3-endo,6-endo,8,9,9,10-heptachlorobornane. Photolysis experiments at λ = 254 nm revealed that B6-913 is photochemicaly the most stable compound of the seven toxaphene compounds studied, with a t1/2 of 213 h. B7-1001, having a t1/2 of 82 h, was the second most stable compound. B8-1412 was degraded more rapidly, with a t1/2 of 28.8 h, than B7-1001, but was still much more stable than P 50 (B9-1679, 2-endo,3-exo,5-endo,6-exo,8,8,9,10,10-nonachlorobornane), which had a t 1/2 of 9.4 h, despite its reputation as a very persistant compound. Under the same experimental conditions hexachlorobenzene (HLB) and octachlorodibenzodioxine (OCDD) were consumed very quickly with t1/2 = 0.0025 and 0.0015 h, respectively.

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

What can I do for you?
Get Best Price

Get Best Price for 51775-36-1