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(1R)-(-)-THIOCAMPHOR

Product Name
(1R)-(-)-THIOCAMPHOR
CAS No.
53402-10-1
Chemical Name
(1R)-(-)-THIOCAMPHOR
Synonyms
(1R)-(-)-THIOCAMPHOR;(1R)-(-)-Thiocamphor;(1R,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2-thione;(1r)-(-)-1,7,7-trimethylbicyclo[2.2.1]heptane-2-thione;Bicyclo[2.2.1]heptane-2-thione, 1,7,7-trimethyl-, (1R,4R)-
CBNumber
CB7169504
Molecular Formula
C10H16S
Formula Weight
168.3
MOL File
53402-10-1.mol
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(1R)-(-)-THIOCAMPHOR Property

Melting point:
136-138 °C(lit.)
Boiling point:
228-230 °C(lit.)
Density 
0.9691 (rough estimate)
refractive index 
1.6500 (estimate)
form 
powder to crystal
color 
Light yellow to Brown
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Safety

Hazard Codes 
F,Xi
Risk Statements 
11-36/37/38
Safety Statements 
16-26-36
RIDADR 
UN 1325 4.1/PG 3
WGK Germany 
3
HS Code 
2930.90.9250
HazardClass 
4.1
PackingGroup 
III
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H228Flammable solid

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P240Ground/bond container and receiving equipment.

P241Use explosion-proof electrical/ventilating/lighting/…/equipment.

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

TCI Chemical
Product number
T1863
Product name
(1R)-(-)-Thiocamphor
Purity
>97.0%(GC)
Packaging
1g
Price
$117
Updated
2024/03/01
TCI Chemical
Product number
T1863
Product name
(1R)-(-)-Thiocamphor
Purity
>97.0%(GC)
Packaging
5g
Price
$355
Updated
2024/03/01
American Custom Chemicals Corporation
Product number
CCH0005078
Product name
(1R)-(-)-THIOCAMPHOR
Purity
95.00%
Packaging
5G
Price
$355.95
Updated
2021/12/16
Chem-Impex
Product number
39147
Product name
(1R)-(-)-Thiocamphor,97%(GC)
Purity
97%(GC)
Packaging
5G
Price
$368.48
Updated
2021/12/16
AK Scientific
Product number
3985AL
Product name
(1R)-(-)-Thiocamphor
Packaging
5g
Price
$498
Updated
2021/12/16
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(1R)-(-)-THIOCAMPHOR Chemical Properties,Usage,Production

Purification Methods

It forms red prisms from EtOH and sublimes under vacuum. It possesses a sulfurous odour and is volatile like camphor. [Sen J Indian Chem Soc 12 647 1935, Sen J Indian Chem Soc 18 76 1941.] The racemate crystallises from *C6H6 and has m 145o [138.6-139o, White & Bishop J Am Chem Soc 62 10 1940]. [Beilstein 7 III 419.]

(1R)-(-)-THIOCAMPHOR Preparation Products And Raw materials

Raw materials

Preparation Products

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(1R)-(-)-THIOCAMPHOR Suppliers

China 22 Germany 1 India 2 Japan 1 Switzerland 1 United Kingdom 1 United States 4 Global 32
TCI Chemicals (India) Pvt. Ltd.
Tel
--
Fax
--
Email
sales-in@tcichemicals.com
Country
India
ProdList
6768
Advantage
58
A.J Chemicals
Tel
--
Fax
--
Email
sales@ajchem.in
Country
India
ProdList
6100
Advantage
58

53402-10-1, (1R)-(-)-THIOCAMPHORRelated Search:

DL-CAMPHORIC ANHYDRIDE (+/-)-EXO EXO-2 3-CAMPHANEDIOL (+)-10-CAMPHORSULFONIMINE (-)-(8,8-DICHLOROCAMPHORYLSULFONYL)OXAZIRIDINE (1S)-(+)-Camphor-10-sulphonic acid (1R)-(-)-10-Camphorsulfonic acid L(-)-10-Camphorsulfonyl chloride Rucaparib Camsylate D-CAMPHOR (-)-CAMPHOR POLYACRYLAMIDOMETHYL BENZYLIDENE CAMPHOR (+)-(8,8-DICHLOROCAMPHORYLSULFONYL)OXAZIRIDINE (7,7-DIMETHYL-2-OXO-BICYCLO[2.2.1]HEPT-1-YL)-METHANESULFONYL CHLORIDE EUROPIUM D-3-TRIFLUOROACETYLCAMPHORATE EUROPIUM TRIS[3-(HEPTAFLUOROPROPYLHYDROXYMETHYLENE)-(+)-CAMPHORATE] L-10-CAMPHORSULFONIC ACID AMMONIUM SALT (1R)-(-)-THIOCAMPHOR thiocamphor

  • (1R)-(-)-THIOCAMPHOR
  • (1r)-(-)-1,7,7-trimethylbicyclo[2.2.1]heptane-2-thione
  • (1R,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2-thione
  • (1<i>R</i>)-(-)-Thiocamphor
  • Bicyclo[2.2.1]heptane-2-thione, 1,7,7-trimethyl-, (1R,4R)-
  • 53402-10-1
  • Organic Building Blocks
  • Thiocarbonyl Compounds
  • Chiral Building Blocks
  • Asymmetric Synthesis
  • Terpenes
  • Bicyclic Monoterpenes
  • Biochemistry
  • Terpenes
  • Bicyclic Monoterpenes