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43000-53-9

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43000-53-9 Usage

Type of compound

Saturated hydrocarbon

Usage

a. Solvent in industrial processes
b. Component in paints, varnishes, and coatings
c. Production of resins, polymers, and other chemical products

Physical properties

a. Strong odor
b. Volatile

Toxicity

Relatively low toxicity

Health hazards

a. Skin irritation
b. Eye irritation
c. Respiratory system irritation

Safety precautions

Proper handling and usage to prevent adverse effects

Check Digit Verification of cas no

The CAS Registry Mumber 43000-53-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,0,0 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 43000-53:
(7*4)+(6*3)+(5*0)+(4*0)+(3*0)+(2*5)+(1*3)=59
59 % 10 = 9
So 43000-53-9 is a valid CAS Registry Number.

43000-53-9SDS

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 Decahydro-1,6-methanonaphthalene

1.2 Other means of identification

Product number -
Other names homoisotwistane

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:43000-53-9 SDS

43000-53-9Relevant articles and documents

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Takaishi,N. et al.

, p. 276 - 281 (1975)

-

-

Takaishi,N. et al.

, p. 825 - 828 (1978)

-

Inflammatory paradentium absorption inhibitor

-

, (2007/10/14)

PROBLEM TO BE SOLVED: To provide an inflammatory alveolar bone resorption inhibitor which can be repeatedly used not only for therapy but also for prevention and has high safeness. SOLUTION: The inflammatory alveolar bone resorption inhibitor comprises 0.01-10 mass% catechins. COPYRIGHT: (C)2009,JPOandINPIT

Reductive Rearrangement with Hydride Transfer of Linearly and Angularly Fused Triquinanes

Kakiuchi, Kiyomi,Ue, Masaki,Kumanoya, Shuichi,Takeuchi, Hideyuki,Tobe, Yoshito,Odaira, Yoshinobu

, p. 1479 - 1482 (2007/10/02)

Relationship between linearly and angularly fused triquinanes is elucidated by reductive rearrangements with hydride transfer of tricyclo2,6>undecan-1-ol, tricyclo1,5>undecan-6-ols, and tricyclo1,5>undecan-11-ol.

ACID CATALYZED RING CONTRACTIONS IN ENDO-2,8-TRIMETHYLENE-CIS-BICYCLOOCTYL CATIONS TO METHYLPERHYDROTRIQUINACENES. ONE OF THE METHYL EXTRUSION PROCESSES IN THE TRICYCLOUNDECANE REARRANGEMENT

Fujikura, Yoshiaki,Takaishi, Naotake,Inamoto, Yoshiaki

, p. 4465 - 4478 (2007/10/02)

Sulfuric acid catalyzed ring contractions with extrusion of a methyl group were examined for alcohol and olefin derivatives (28-31) of endo-2,8-trimethylene-cis-bicyclooctane (11), which was one of the two possible progenitors, among altogether 69

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