Synonym: (+)-Camphoric acid; (1R,3S)-1,2,2-Trimethyl-1,3-cyclopentanedicarboxylic acid
CAS Number: 124-83-4
Empirical Formula (Hill Notation): C10H16O4
Molecular Weight: 200.23
EC Number: 204-715-0
MDL Number: MFCD00001375
Linear Formula: C10H16O4
Product Type: Chemical
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.
This image depicts SKU: C409-100G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.
This image depicts SKU: C409-5G
| assay |
99% |
| form |
powder |
| InChI |
1S/C10H16O4/c1-9(2)6(7(11)12)4-5-10(9,3)8(13)14/h6H,4-5H2,1-3H3,(H,11,12)(H,13,14)/t6-,10+/m1/s1 |
| InChI key |
LSPHULWDVZXLIL-LDWIPMOCSA-N |
| mp |
183-186 °C (lit.) |
| optical activity |
[α]20/D 46°, c = 1 in ethanol |
| Quality Level |
200  |
| SMILES string |
CC1(C)[C@H](CC[C@@]1(C)C(O)=O)C(O)=O |
| Application: |
(1R,3S)-(+)-Camphoric acid may be used in the preparation (1R,2S,3R,5S)-2,3-dibenzyl-1,8,8-trimethyl-3-thianiumbicyclo[3.2.1]octane perchlorate. It reacts with uranyl nitrate in pyridine(py) or py/methanol(MeOH) to form novel uranyl-organic assemblages. |
| General description: |
Camphoric acid is a diacid, generally prepared by the oxidation of terpene (+)-camphor. It can be used as a chirality inducing agent in some organic reactions. |
| Packaging: |
5, 100 g in poly bottle |
| Symbol |
GHS07 |
| Signal word |
Warning |
| Hazard statements |
H302 |
| Hazard Codes |
Xn |
| Risk Statements |
22 |
| RIDADR |
NONH for all modes of transport |
| WGK Germany |
WGK 2 |
| Flash Point(F) |
Not applicable |
| Flash Point(C) |
Not applicable |
| Purity |
99% |
| mp |
183-186 °C (lit.) |
| UNSPSC |
51113400 |