午夜插插,噜噜噜影院,啪啪伊人网,欧美熟夫,景甜吻戏视频,男人强操性感蕾丝美女视频在线网站,日本美女跳舞视频

Home Cart 0 Sign in  

[ CAS No. 770-69-4 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 770-69-4
Chemical Structure| 770-69-4
Structure of 770-69-4 * Storage: {[proInfo.prStorage]}

Please Login or Create an Account to: See VIP prices and availability

Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Search after Editing

* Storage: {[proInfo.prStorage]}

* Shipping: {[proInfo.prShipping]}

Quality Control of [ 770-69-4 ]

Related Doc. of [ 770-69-4 ]

Alternatived Products of [ 770-69-4 ]
Product Citations

Product Details of [ 770-69-4 ]

CAS No. :770-69-4 MDL No. :MFCD00142626
Formula : C12H20 Boiling Point : No data available
Linear Structure Formula :- InChI Key :LXTHCCWEYOKFSR-UHFFFAOYSA-N
M.W : 164.29 Pubchem ID :522637
Synonyms :

Safety of [ 770-69-4 ]

Signal Word:Warning Class:
Precautionary Statements:P210-P264-P270-P280-P301+P312-P330-P370+P378-P403+P235-P501 UN#:
Hazard Statements:H227-H302 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 770-69-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 770-69-4 ]

[ 770-69-4 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 1678-91-7 ]
  • [ 702-79-4 ]
  • [ 1687-36-1 ]
  • [ 493-02-7 ]
  • [ 770-69-4 ]
  • [ 707-35-7 ]
  • [ 768-91-2 ]
  • 2
  • [ 696-29-7 ]
  • [ 702-79-4 ]
  • [ 1687-36-1 ]
  • [ 493-02-7 ]
  • [ 770-69-4 ]
  • [ 707-35-7 ]
  • [ 768-91-2 ]
  • 3
  • [ 1678-98-4 ]
  • [ 702-79-4 ]
  • [ 1687-36-1 ]
  • [ 493-02-7 ]
  • [ 770-69-4 ]
  • [ 707-35-7 ]
  • [ 768-91-2 ]
  • 4
  • [ 82166-21-0 ]
  • [ 702-79-4 ]
  • [ 1687-36-1 ]
  • [ 493-02-7 ]
  • [ 770-69-4 ]
  • [ 707-35-7 ]
  • [ 768-91-2 ]
YieldReaction ConditionsOperation in experiment
(2) Reaction Into a 100 ml content autoclave, 2.0 grams of zeolite prepared as above and 2.0 grams of tetracyclo-(6.2.1.13,6.02,7) dodecane were placed quickly and after evacuation hydrogen chloride gas was introduced to 1.5 kg/cm2 followed by hydrogen gas to total pressure of 30 kg/cm2. The reaction was carried out for 4 hours at 250 C. with stirring. After the reaction, n-tridecane was added to the reaction mixture and then the catalyst (zeolite) and the reaction solution was separated by filtration. The reaction solution was analyzed using p-cymene as the internal standard by gas chromatography. As the result, conversion yield of tetracyclo-(6.2.1.13,6.02,7) dodecane, selectivity of 1,3-dimethyl adamantane, yield of 1,3-dimethyl adamantane, selectivity of 1-ethyl adamantane, and yield of 1-ethyl adamantane were 21.5%, 9.3%, 2.0%, 15.2% and 3.3%, respectively.
  • 7
  • [ 2146-36-3 ]
  • [ 702-79-4 ]
  • [ 770-69-4 ]
YieldReaction ConditionsOperation in experiment
77%; 15% With hydrogen fluoride; boron trifluoride; at 100℃; for 4h;Autoclave; Example 1 [0040] PHA was subjected to an isomerization reaction by use of a Hastelloy autoclave having a capacity of 0.5 L and including an electromagnetic stirring device, a heating device, a gas and liquid supply opening and a reaction product discharge opening. 50 g (2.5 mol) of HF produced by Morita Chemical Industries Co., Ltd. and 100 g (0.6 mol) of PHA were put to a reactor, and 16 g (0.24 mol) of BF3 produced by Stella Chemifa Corporation was supplied. Then, these substances were heated to a temperature of 100 C. by the heating device with no solvent, and stirred for 4 hours while the temperature was kept at 100 C. The reaction product solution was sampled. The yield of 1,3-dimethyladamantane was 77% with respect to PHA as the material. The yield of 1-ethyladamantane as an intermediate was 15% with respect to PHA as the material, while no high boiling point compound was observed. Then, as a result of being left still, the reaction product solution was divided into two layers, namely, an organic layer containing 1,3-dimethyladamantane and a catalyst layer. The catalyst layer was obtained by liquid-liquid separation. The separated catalyst layer was supplied to a distillation tower in which heptane was circulated. As a result, almost all the amount of BF3 was recovered from a top part of the tower, and almost all the amount of HF was recovered from a condenser in the top part of the tower.
  • 9
  • [ 58865-53-5 ]
  • [ 702-79-4 ]
  • [ 770-69-4 ]
  • [ 16267-35-9 ]
  • 10
  • [ 702-79-4 ]
  • [ 16207-81-1 ]
  • [ 770-69-4 ]
  • [ 16267-35-9 ]
Recommend Products
Same Skeleton Products

Technical Information

Historical Records

Related Functional Groups of
[ 770-69-4 ]

Aliphatic Cyclic Hydrocarbons

Chemical Structure| 16267-35-9

[ 16267-35-9 ]

1,4-Dimethyladamantane

Similarity: 1.00

Chemical Structure| 707-35-7

[ 707-35-7 ]

1,3,5-Trimethyladamantane

Similarity: 1.00

Chemical Structure| 3732-31-8

[ 3732-31-8 ]

1,1'-Bi(adamantane)

Similarity: 1.00

Chemical Structure| 768-91-2

[ 768-91-2 ]

1-Methyladamantane

Similarity: 1.00

Chemical Structure| 26527-76-4

[ 26527-76-4 ]

(3,4-Dimethylhexane-3,4-diyl)dicyclohexane

Similarity: 1.00

; ;