ChemicalBook > CAS DataBase List > (1R)-CAMPHOR OXIME

(1R)-CAMPHOR OXIME

Product Name
(1R)-CAMPHOR OXIME
CAS No.
2792-42-9
Chemical Name
(1R)-CAMPHOR OXIME
Synonyms
D-CAMPHOR OXIME;2-Norbornyl oxime;(+)-Camphor oxime;(1R)-CAMPHOR OXIME;camphor,oxime,(1R)-;Camphor, oxime, (1R)-;(1R)-Camphor Oxime >(1R)-CAMPHOR OXIME 98+%;(1R)-Camphor Oxime;(1R,4R)-Bornane-2-oneoxime
CBNumber
CB3680009
Molecular Formula
C10H17NO
Formula Weight
167.25
MOL File
2792-42-9.mol
More
Less

(1R)-CAMPHOR OXIME Property

Melting point:
115-119 °C
solubility 
almost transparency in Methanol
form 
powder to crystal
color 
White to Almost white
optical activity
[α]20/D 40.5±1°, c = 5% in ethanol
BRN 
2413664
InChI
1S/C10H17NO/c1-9(2)7-4-5-10(9,3)8(6-7)11-12/h7,12H,4-6H2,1-3H3/b11-8+/t7-,10+/m1/s1
InChIKey
OVFDEGGJFJECAT-RZIOALPKSA-N
SMILES
CC1(C)[C@@H]2CC[C@@]1(C)C(\C2)=N\O
CAS DataBase Reference
2792-42-9(CAS DataBase Reference)
EPA Substance Registry System
Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, oxime, (1R,4R)- (2792-42-9)
More
Less

Safety

Safety Statements 
22-24/25
WGK Germany 
3
TSCA 
TSCA listed
HS Code 
2929900090
Storage Class
11 - Combustible Solids
More
Less

Hazard and Precautionary Statements (GHS)

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
21335
Product name
(1R)-Camphor oxime
Purity
≥97.0% (sum of enantiomers, GC)
Packaging
5G
Price
$82
Updated
2023/06/20
TCI Chemical
Product number
C0013
Product name
(1R)-Camphor Oxime
Purity
>98.0%(GC)
Packaging
1g
Price
$28
Updated
2025/07/31
TCI Chemical
Product number
C0013
Product name
(1R)-Camphor Oxime
Purity
>98.0%(GC)
Packaging
25g
Price
$249
Updated
2025/07/31
TCI Chemical
Product number
C0013
Product name
(1R)-Camphor Oxime
Purity
>98.0%(GC)
Packaging
5g
Price
$84
Updated
2025/07/31
Chem-Impex
Product number
39179
Product name
(1R)-Camphoroxime,≥98%(GC)
Purity
≥98%(GC)
Packaging
5G
Price
$99.01
Updated
2021/12/16
More
Less

(1R)-CAMPHOR OXIME Chemical Properties,Usage,Production

Synthesis

In 500 liters of reaction kettle add camphor 50 grams, sodium methanol 43.2Kg and 80Kg ethanol, ice water cooling through 34Kg ethyl nitrite, aeration is completed to continue the reaction for 2 hours, add 100Kg of water, liquid separation, the lower layer of the solution with 10% hydrochloric acid and neutralization to the PH value of 1-2, extracted with 100Kg of dichloromethane two times, combined with the dichloromethane, dechlorination of dichloromethane, recrystallization with ethanol to get a light yellow solid camphor oxime 50kg, yield 84%. Ethanol recrystallization to get light yellow solid camphor oxime 50kg, yield 84%.

(1R)-CAMPHOR OXIME Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

(1R)-CAMPHOR OXIME Suppliers

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Shanghai Longsheng chemical Co.,Ltd.
Tel
021-58099652-8005 13585536065
Fax
021-58099609
Email
bin.wu@shlschem.com
Country
China
ProdList
9892
Advantage
59
Shandong Xiya Chemical Co., Ltd
Tel
13355009207 13355009207
Fax
0539-6365991
Email
3007715519@qq.com
Country
China
ProdList
18729
Advantage
57
Maya High Purity Chemicals
Tel
+86 (573) 82222445 (0)18006601000 452520369
Fax
+86 (573) 82222643
Email
sales@maya-r.com
Country
China
ProdList
11707
Advantage
57
Chengdu Ai Keda Chemical Technology Co., Ltd.
Tel
4008-755-333 18080918076
Fax
028-86757656
Email
800078821@qq.com
Country
China
ProdList
9718
Advantage
55
Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.
Tel
025-66113011 17798518460
Fax
(1)02557626880
Email
cfzhang@aikonchem.com
Country
China
ProdList
19906
Advantage
55
TOKYO CHEMICAL INDUSTRY CO., LTD.
Tel
03-36680489
Fax
03-3668-0520
Email
Sales-JP@TCIchemicals.com
Country
Japan
ProdList
28387
Advantage
80
TCI Europe
Tel
320-37350700
Fax
+32 (0)37350701
Email
sales@tcieurope.eu
Country
Europe
ProdList
23671
Advantage
75

2792-42-9, (1R)-CAMPHOR OXIMERelated Search:


  • D-CAMPHOR OXIME
  • (1R)-CAMPHOR OXIME
  • (+)-Camphor oxime
  • (2E)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one oxime
  • 1,7,7-trimethyl-,oxime,(1theta)-bicyclo[2.2.1]heptan-2-on
  • 2-Norbornyl oxime
  • bicyclo[2.2.1]heptan-2-one,1,7,7-trimethyl-,oxime,(1R)-
  • Camphor, oxime, (1R)-
  • camphor,oxime,(1R)-
  • (1R)-1,7,7-TRIMETHYLBICYCLO[2,2,1]HEPTAN-2-ONE OXIME
  • (1R)-1,7,7-Trimethylbicylco[2,2,1]heptan-2-one oxime
  • (1R)-CAMPHOR OXIME 98+%
  • (1<i>R</i>)-Camphor Oxime
  • (1R,4R)-Bornane-2-oneoxime
  • [1R,4R,(+)]-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one oxime
  • (NE)-N-[(4R)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanylidene]hydroxylamine
  • Bicyclo[2.2.1]heptan-2-one,1,7,7-trimethyl-, oxime, (1R,4R)-
  • (1R)-Camphor Oxime &gt
  • (1R,E)-1,7,7-trimethylbicyclo[2.2.1]Heptan-2-one oxime
  • 2792-42-9
  • C9H16CNOH
  • Chiral Building Blocks
  • Asymmetric Synthesis
  • Terpenes
  • Bicyclic Monoterpenes
  • Oximes
  • Organic Building Blocks
  • Bicyclic Monoterpenes
  • Biochemistry
  • Terpenes